Repeat expansion in C9ORF72 is not a major cause of amyotrophic lateral sclerosis among Iranian patients-Reference-Cited by-同舟云学术

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Repeat expansion in C9ORF72 is not a major cause of amyotrophic lateral sclerosis among Iranian patients

Published:2014-01 Issue:1 Volume:35 Page:267.e1-267.e7
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Alavi Afagh,Nafissi Shahriar,Rohani Mohammad,Shahidi Gholamali,Zamani Babak,Shamshiri Hosein,Safari Iman,Elahi Elahe

Funder

Tehran University of Medical Sciences

Iran National Science Foundation

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

Reference64 articles.

1. Genetic analysis and SOD1 mutation screening in Iranian amyotrophic lateral sclerosis patients;Alavi;Neurobiol. Aging,2013

2. Amyotrophic lateral sclerosis associated with mutations in the CuZn superoxide dismutase gene;Andersen;Curr. Neurol. Neurosci. Rep.,2006

3. Clinical genetics of amyotrophic lateral sclerosis: what do we really know?;Andersen;Nat. Rev. Neurol.,2011

4. Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patients;Andersen;Brain,1996

5. Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase;Andersen;Nat. Genet.,1995

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2. Analysis of C9orf72 repeat expansions in Georgian patients with Amyotrophic lateral sclerosis (ALS);F1000Research;2023-09-07

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