Correction: Phenotype and Genotype Heterogeneity of Pla2g6-Associated Neurodegeneration in a Cohort of Pediatric and Adult Patients (Orphanet Journal of Rare Diseases, (2023), 18, 1, (177), 10.1186/S13023-023-02780-9)

Correction: Phenotype and Genotype Heterogeneity of Pla2g6-Associated Neurodegeneration in a Cohort of Pediatric and Adult Patients (Orphanet Journal of Rare Diseases, (2023), 18, 1, (177), 10.1186/S13023-023-02780-9) Publisher Pubmed

Dehnavi AZ¹ ; Bemanalizadeh M^{1, 2} ; Kahani SM³ ; Ashrafi MR¹ ; Rohani M^{4, 5} ; Toosi MB^{6, 7} ; Heidari M¹ ; Hosseinpour S¹ ; Amini B¹ ; Zokaei S^{8, 9} ; Rezaei Z¹ ; Aryan H^{8, 10} ; Amanat M¹¹ ; Vahidnezhad H^{12, 13} Show All Authors

Dehnavi AZ¹
Bemanalizadeh M^{1, 2}
Kahani SM³
Ashrafi MR¹
Rohani M^{4, 5}
Toosi MB^{6, 7}
Heidari M¹
Hosseinpour S¹
Amini B¹
Zokaei S^{8, 9}
Rezaei Z¹
Aryan H^{8, 10}
Amanat M¹¹
Vahidnezhad H^{12, 13}
Mohammadi P^{3, 14}
Garshasbi M³
Tavasoli AR^{1, 12, 14}

Show Affiliations

1. Department of Pediatrics, Division of Pediatric Neurology, Children’s Medical Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran
2. Child Growth and Development Research Center, Research Institute for Primordial Prevention of Non-Communicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran
3. Faculty of Medical Sciences, Department of Medical Genetics, Tarbiat Modares University, Tehran, Iran
4. Skull Base Research Center, The Five Senses Health Institute, Rasoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran
5. Department of Neurology, Rasoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran
6. Department of Pediatrics, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
7. Neuroscience Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
8. Dr. Farhud’s Genetic Clinic, Tehran, Iran
9. School of Advanced Medical Science, Islamic Azad University, Tehran, Iran
10. National Institute of Genetic Engineering and Biotechnology, Tehran, Iran
11. Department of Neurology, Johns Hopkins Medicine, Baltimore, MD, United States
12. Jefferson Institute of Molecular Medicine, Thomas Jefferson University, Philadelphia, PA, United States
13. Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA, United States
14. Pediatric Neurology Division, Children’s Medical Center, Pediatrics Center of Excellence, Ataxia Clinic, Tehran University of Medical Sciences, Tehran, Iran

Source: Orphanet Journal of Rare Diseases Published:2023

Abstract

Following publication of the original article [1], we have been notified that the sentence on equal contribution of the first authors was missed. It should be as follows: Ali Zare Dehanavi and Maryam Bemanalizadeh have contributed equally to this work. © 2023, The Author(s).

Style	Citing Format
MLA	Dehnavi AZ, et al.. "Correction: Phenotype and Genotype Heterogeneity of Pla2g6-Associated Neurodegeneration in a Cohort of Pediatric and Adult Patients (Orphanet Journal of Rare Diseases, (2023), 18, 1, (177), 10.1186/S13023-023-02780-9)." Orphanet Journal of Rare Diseases, vol. 18, no. 1, 2023, pp. -.
APA	Dehnavi AZ, Bemanalizadeh M, Kahani SM, Ashrafi MR, Rohani M, Toosi MB, Heidari M, Hosseinpour S, Amini B, Zokaei S, Rezaei Z, Aryan H, Amanat M, Vahidnezhad H, Mohammadi P, Garshasbi M, Tavasoli AR (2023). Correction: Phenotype and Genotype Heterogeneity of Pla2g6-Associated Neurodegeneration in a Cohort of Pediatric and Adult Patients (Orphanet Journal of Rare Diseases, (2023), 18, 1, (177), 10.1186/S13023-023-02780-9). Orphanet Journal of Rare Diseases, 18(1), -.
Chicago	Dehnavi AZ, Bemanalizadeh M, Kahani SM, Ashrafi MR, Rohani M, Toosi MB, Heidari M, et al.. "Correction: Phenotype and Genotype Heterogeneity of Pla2g6-Associated Neurodegeneration in a Cohort of Pediatric and Adult Patients (Orphanet Journal of Rare Diseases, (2023), 18, 1, (177), 10.1186/S13023-023-02780-9)." Orphanet Journal of Rare Diseases 18, no. 1 (2023): -.
Harvard	Dehnavi AZ et al. (2023) 'Correction: Phenotype and Genotype Heterogeneity of Pla2g6-Associated Neurodegeneration in a Cohort of Pediatric and Adult Patients (Orphanet Journal of Rare Diseases, (2023), 18, 1, (177), 10.1186/S13023-023-02780-9)', Orphanet Journal of Rare Diseases, 18(1), pp. -.
Vancouver	Dehnavi AZ, Bemanalizadeh M, Kahani SM, Ashrafi MR, Rohani M, Toosi MB, et al.. Correction: Phenotype and Genotype Heterogeneity of Pla2g6-Associated Neurodegeneration in a Cohort of Pediatric and Adult Patients (Orphanet Journal of Rare Diseases, (2023), 18, 1, (177), 10.1186/S13023-023-02780-9). Orphanet Journal of Rare Diseases. 2023;18(1):-.
BibTex	@article{ author = {Dehnavi AZ and Bemanalizadeh M and Kahani SM and Ashrafi MR and Rohani M and Toosi MB and Heidari M and Hosseinpour S and Amini B and Zokaei S and Rezaei Z and Aryan H and Amanat M and Vahidnezhad H and Mohammadi P and Garshasbi M and Tavasoli AR}, title = {Correction: Phenotype and Genotype Heterogeneity of Pla2g6-Associated Neurodegeneration in a Cohort of Pediatric and Adult Patients (Orphanet Journal of Rare Diseases, (2023), 18, 1, (177), 10.1186/S13023-023-02780-9)}, journal = {Orphanet Journal of Rare Diseases}, volume = {18}, number = {1}, pages = {-}, year = {2023} }
RIS	TY - JOUR AU - Dehnavi AZ AU - Bemanalizadeh M AU - Kahani SM AU - Ashrafi MR AU - Rohani M AU - Toosi MB AU - Heidari M AU - Hosseinpour S AU - Amini B AU - Zokaei S AU - Rezaei Z AU - Aryan H AU - Amanat M AU - Vahidnezhad H AU - Mohammadi P AU - Garshasbi M AU - Tavasoli AR TI - Correction: Phenotype and Genotype Heterogeneity of Pla2g6-Associated Neurodegeneration in a Cohort of Pediatric and Adult Patients (Orphanet Journal of Rare Diseases, (2023), 18, 1, (177), 10.1186/S13023-023-02780-9) JO - Orphanet Journal of Rare Diseases VL - 18 IS - 1 SP - EP - PY - 2023 ER -

Style

Citing Format

MLA

Dehnavi AZ, et al.. "Correction: Phenotype and Genotype Heterogeneity of Pla2g6-Associated Neurodegeneration in a Cohort of Pediatric and Adult Patients (Orphanet Journal of Rare Diseases, (2023), 18, 1, (177), 10.1186/S13023-023-02780-9)." Orphanet Journal of Rare Diseases, vol. 18, no. 1, 2023, pp. -.

APA

Dehnavi AZ, Bemanalizadeh M, Kahani SM, Ashrafi MR, Rohani M, Toosi MB, Heidari M, Hosseinpour S, Amini B, Zokaei S, Rezaei Z, Aryan H, Amanat M, Vahidnezhad H, Mohammadi P, Garshasbi M, Tavasoli AR (2023). Correction: Phenotype and Genotype Heterogeneity of Pla2g6-Associated Neurodegeneration in a Cohort of Pediatric and Adult Patients (Orphanet Journal of Rare Diseases, (2023), 18, 1, (177), 10.1186/S13023-023-02780-9). Orphanet Journal of Rare Diseases, 18(1), -.

Chicago

Dehnavi AZ, Bemanalizadeh M, Kahani SM, Ashrafi MR, Rohani M, Toosi MB, Heidari M, et al.. "Correction: Phenotype and Genotype Heterogeneity of Pla2g6-Associated Neurodegeneration in a Cohort of Pediatric and Adult Patients (Orphanet Journal of Rare Diseases, (2023), 18, 1, (177), 10.1186/S13023-023-02780-9)." Orphanet Journal of Rare Diseases 18, no. 1 (2023): -.

Harvard

Dehnavi AZ et al. (2023) 'Correction: Phenotype and Genotype Heterogeneity of Pla2g6-Associated Neurodegeneration in a Cohort of Pediatric and Adult Patients (Orphanet Journal of Rare Diseases, (2023), 18, 1, (177), 10.1186/S13023-023-02780-9)', Orphanet Journal of Rare Diseases, 18(1), pp. -.

Vancouver

Dehnavi AZ, Bemanalizadeh M, Kahani SM, Ashrafi MR, Rohani M, Toosi MB, et al.. Correction: Phenotype and Genotype Heterogeneity of Pla2g6-Associated Neurodegeneration in a Cohort of Pediatric and Adult Patients (Orphanet Journal of Rare Diseases, (2023), 18, 1, (177), 10.1186/S13023-023-02780-9). Orphanet Journal of Rare Diseases. 2023;18(1):-.

BibTex

@article{ author = {Dehnavi AZ and Bemanalizadeh M and Kahani SM and Ashrafi MR and Rohani M and Toosi MB and Heidari M and Hosseinpour S and Amini B and Zokaei S and Rezaei Z and Aryan H and Amanat M and Vahidnezhad H and Mohammadi P and Garshasbi M and Tavasoli AR}, title = {Correction: Phenotype and Genotype Heterogeneity of Pla2g6-Associated Neurodegeneration in a Cohort of Pediatric and Adult Patients (Orphanet Journal of Rare Diseases, (2023), 18, 1, (177), 10.1186/S13023-023-02780-9)}, journal = {Orphanet Journal of Rare Diseases}, volume = {18}, number = {1}, pages = {-}, year = {2023} }

RIS

TY - JOUR
AU - Dehnavi AZ
AU - Bemanalizadeh M
AU - Kahani SM
AU - Ashrafi MR
AU - Rohani M
AU - Toosi MB
AU - Heidari M
AU - Hosseinpour S
AU - Amini B
AU - Zokaei S
AU - Rezaei Z
AU - Aryan H
AU - Amanat M
AU - Vahidnezhad H
AU - Mohammadi P
AU - Garshasbi M
AU - Tavasoli AR
TI - Correction: Phenotype and Genotype Heterogeneity of Pla2g6-Associated Neurodegeneration in a Cohort of Pediatric and Adult Patients (Orphanet Journal of Rare Diseases, (2023), 18, 1, (177), 10.1186/S13023-023-02780-9)
JO - Orphanet Journal of Rare Diseases
VL - 18
IS - 1
SP -
EP -
PY - 2023
ER -

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Authors

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Abstract