Genetic causes of amyotrophic lateral sclerosis: New genetic analysis methodologies entailing new opportunities and challenges-Reference-Cited by-同舟云学术

Genetic causes of amyotrophic lateral sclerosis: New genetic analysis methodologies entailing new opportunities and challenges

Published:2015-05 Issue: Volume:1607 Page:75-93
ISSN:0006-8993
Container-title:Brain Research
language:en
Short-container-title:Brain Research

Author:

Marangi Giuseppe,Traynor Bryan J.

Publisher

Elsevier BV

Subject

Developmental Biology,Neurology (clinical),Molecular Biology,General Neuroscience

Reference198 articles.

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2. Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy;Ajroud-Driss;Neurogenetics,2014

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

4. Repeat expansion in C9ORF72 is not a major cause of amyotrophic lateral sclerosis among Iranian patients;Alavi;Neurobiol. Aging,2014

5. Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome;Albers;Nat. Genet.,2012

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