A Founder Mutation in Coq7, P.(Leu111pro), Causes Pure Hereditary Spastic Paraplegia (Hsp) in the Iranian Population

A Founder Mutation in Coq7, P.(Leu111pro), Causes Pure Hereditary Spastic Paraplegia (Hsp) in the Iranian Population Publisher Pubmed

Sadr Z¹ ; Zareabdollahi D¹ ; Rohani M² ; Alavi A^{1, 3}

Show Affiliations

1. Genetics research center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
2. Department of Neurology, Iran University of Medical Sciences, Hazrat Rasool Hospital, Tehran, Iran
3. Neuromuscular Research Center, Tehran University of Medical Sciences, Tehran, Iran

Source: Neurological Sciences Published:2023

Abstract

[No abstract available]

Related Docs

1. Clinical Spectrum in Multiple Families With Primary Coq10 Deficiency, American Journal of Medical Genetics# Part A (2021)

2. Adolescence Onset Primary Coenzyme Q10 Deficiency With Rare Coq8a Gene Mutation: A Case Report and Review of Literature, Clinical Medicine Insights: Case Reports (2023)

Experts (# of related papers)

Mohammad Kazem Bakhshandeh-Bali (1)

Style	Citing Format
MLA	Sadr Z, et al.. "A Founder Mutation in Coq7, P.(Leu111pro), Causes Pure Hereditary Spastic Paraplegia (Hsp) in the Iranian Population." Neurological Sciences, vol. 44, no. 7, 2023, pp. 2599-2602.
APA	Sadr Z, Zareabdollahi D, Rohani M, Alavi A (2023). A Founder Mutation in Coq7, P.(Leu111pro), Causes Pure Hereditary Spastic Paraplegia (Hsp) in the Iranian Population. Neurological Sciences, 44(7), 2599-2602.
Chicago	Sadr Z, Zareabdollahi D, Rohani M, Alavi A. "A Founder Mutation in Coq7, P.(Leu111pro), Causes Pure Hereditary Spastic Paraplegia (Hsp) in the Iranian Population." Neurological Sciences 44, no. 7 (2023): 2599-2602.
Harvard	Sadr Z et al. (2023) 'A Founder Mutation in Coq7, P.(Leu111pro), Causes Pure Hereditary Spastic Paraplegia (Hsp) in the Iranian Population', Neurological Sciences, 44(7), pp. 2599-2602.
Vancouver	Sadr Z, Zareabdollahi D, Rohani M, Alavi A. A Founder Mutation in Coq7, P.(Leu111pro), Causes Pure Hereditary Spastic Paraplegia (Hsp) in the Iranian Population. Neurological Sciences. 2023;44(7):2599-2602.
BibTex	@article{ author = {Sadr Z and Zareabdollahi D and Rohani M and Alavi A}, title = {A Founder Mutation in Coq7, P.(Leu111pro), Causes Pure Hereditary Spastic Paraplegia (Hsp) in the Iranian Population}, journal = {Neurological Sciences}, volume = {44}, number = {7}, pages = {2599-2602}, year = {2023} }
RIS	TY - JOUR AU - Sadr Z AU - Zareabdollahi D AU - Rohani M AU - Alavi A TI - A Founder Mutation in Coq7, P.(Leu111pro), Causes Pure Hereditary Spastic Paraplegia (Hsp) in the Iranian Population JO - Neurological Sciences VL - 44 IS - 7 SP - 2599 EP - 2602 PY - 2023 ER -

Science Communicator Platform

Authors

Authors Affiliations

Abstract