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A founder mutation in COQ7, p.(Leu111Pro), causes pure hereditary spastic paraplegia (HSP) in the Iranian population.
Sadr, Zahra; Zare-Abdollahi, Davood; Rohani, Mohammad; Alavi, Afagh.
  • Sadr Z; Genetics research center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Zare-Abdollahi D; Genetics research center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Rohani M; Department of Neurology, Iran University of Medical Sciences, Hazrat Rasool Hospital, Tehran, Iran.
  • Alavi A; Genetics research center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. afaghalavi@gmail.com.
Neurol Sci ; 44(7): 2599-2602, 2023 07.
Article en En | MEDLINE | ID: mdl-36854932
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria Tipo de estudio: Etiology_studies Límite: Humans País como asunto: Asia Idioma: En Año: 2023 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria Tipo de estudio: Etiology_studies Límite: Humans País como asunto: Asia Idioma: En Año: 2023 Tipo del documento: Article