An Iranian familial amyotrophic lateral sclerosis pedigree with p.Val48Phe causing mutation in SOD1: a genetic and clinical report

OBJECTIVE(S): Amyotrophic lateral sclerosis (ALS), a fatal progressive neurodegenerative disorder, is the most common motor neuron disease in European populations. Approximately 10% of ALS cases are familial (FALS) and the other patients are considered as sporadic ALS (SALS). Among many ALS causing...

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Vydáno v:Iran J Basic Med Sci
Hlavní autoři: Alavi, Afagh, Khani, Marzieh, Nafissi, Shahriar, Shamshiri, Hosein, Elahi, Elahe
Médium: Artigo
Jazyk:Inglês
Vydáno: Mashhad University of Medical Sciences 2014
Témata:
Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4340979/
https://ncbi.nlm.nih.gov/pubmed/25729540
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