ARHGEF28 gene exon 6/intron 6 junction mutations in Chinese amyotrophic lateral sclerosis cohort-Reference-Cited by-同舟云学术

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ARHGEF28 gene exon 6/intron 6 junction mutations in Chinese amyotrophic lateral sclerosis cohort

Published:2014-04-08 Issue:3-4 Volume:15 Page:309-311
ISSN:2167-8421
Container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
language:en
Short-container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Author:

Ma Yan,Tang Lu,Chen Lu,Zhang Bin,Deng Pan,Wang Jingran,Yang Yi,Liu Rong,Yang Yan,Ye Shan,Liu Xiaolu,Zhang Huagang,Fan Dongsheng

Publisher

Informa UK Limited

Subject

Neurology (clinical),Neurology

Link

http://www.tandfonline.com/doi/pdf/10.3109/21678421.2014.896926

Reference5 articles.

1. Clinical genetics of amyotrophic lateral sclerosis: what do we really know?

2. ATXN2 CAG repeat expansions increase the risk for Chinese patients with amyotrophic lateral sclerosis

3. A rare Cu/Zn superoxide dismutase mutation causing familial amyotrophic lateral sclerosis with variable age of onset and incomplete penetrance in China

4. Human low molecular weight neurofilament (NFL) mRNA interacts with a predicted p190RhoGEF homologue (RGNEF) in humans

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