Identification of a Large Homozygous Vps13c Deletion in a Patient With Early-Onset Parkinsonism

Identification of a Large Homozygous Vps13c Deletion in a Patient With Early-Onset Parkinsonism Publisher Pubmed

Darvish H¹ ; Bravo P² ; Tafakhori A³ ; Azcona LJ^{2, 4} ; Ranjiburachaloo S³ ; Johari AH¹ ; Paisanruiz C^{2, 5, 6, 7, 8}

Show Affiliations

1. Department of Medical Genetics, Semnan University of Medical Sciences, Semnan, Iran
2. Department of Neurology, Icahn School of Medicine at Mount Sinai, One Gustave L, New York, NY, United States
3. Iranian Center of Neurological Research, Neuroscience institute, Tehran University of Medical Sciences, Tehran, Iran
4. Department of Neurosciences, Icahn School of Medicine at Mount Sinai, New York, NY, United States
5. Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, United States
6. Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, United States
7. The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States
8. The Friedman Brain and Mindich Child Health and Development Institutes, Icahn School of Medicine at Mount Sinai, New York, NY, United States

Source: Movement Disorders Published:2018

Abstract

[No abstract available]

Related Docs

1. Molecular Characterization of Prkn Structural Variations Identified Through Whole-Genome Sequencing, Molecular Genetics and Genomic Medicine (2018)

2. A Clinical and Molecular Genetic Study of 50 Families With Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations, Molecular Neurobiology (2018)

Experts (# of related papers)

Abbas Tafakhori (2)

Style	Citing Format
MLA	Darvish H, et al.. "Identification of a Large Homozygous Vps13c Deletion in a Patient With Early-Onset Parkinsonism." Movement Disorders, vol. 33, no. 12, 2018, pp. 1968-1970.
APA	Darvish H, Bravo P, Tafakhori A, Azcona LJ, Ranjiburachaloo S, Johari AH, Paisanruiz C (2018). Identification of a Large Homozygous Vps13c Deletion in a Patient With Early-Onset Parkinsonism. Movement Disorders, 33(12), 1968-1970.
Chicago	Darvish H, Bravo P, Tafakhori A, Azcona LJ, Ranjiburachaloo S, Johari AH, Paisanruiz C. "Identification of a Large Homozygous Vps13c Deletion in a Patient With Early-Onset Parkinsonism." Movement Disorders 33, no. 12 (2018): 1968-1970.
Harvard	Darvish H et al. (2018) 'Identification of a Large Homozygous Vps13c Deletion in a Patient With Early-Onset Parkinsonism', Movement Disorders, 33(12), pp. 1968-1970.
Vancouver	Darvish H, Bravo P, Tafakhori A, Azcona LJ, Ranjiburachaloo S, Johari AH, et al.. Identification of a Large Homozygous Vps13c Deletion in a Patient With Early-Onset Parkinsonism. Movement Disorders. 2018;33(12):1968-1970.
BibTex	@article{ author = {Darvish H and Bravo P and Tafakhori A and Azcona LJ and Ranjiburachaloo S and Johari AH and Paisanruiz C}, title = {Identification of a Large Homozygous Vps13c Deletion in a Patient With Early-Onset Parkinsonism}, journal = {Movement Disorders}, volume = {33}, number = {12}, pages = {1968-1970}, year = {2018} }
RIS	TY - JOUR AU - Darvish H AU - Bravo P AU - Tafakhori A AU - Azcona LJ AU - Ranjiburachaloo S AU - Johari AH AU - Paisanruiz C TI - Identification of a Large Homozygous Vps13c Deletion in a Patient With Early-Onset Parkinsonism JO - Movement Disorders VL - 33 IS - 12 SP - 1968 EP - 1970 PY - 2018 ER -

Science Communicator Platform

Authors

Authors Affiliations

Abstract