SOD1, ANG, TARDBP and FUS mutations in amyotrophic lateral sclerosis: A United States clinical testing lab experience-Reference-Cited by-同舟云学术

SOD1, ANG, TARDBP and FUS mutations in amyotrophic lateral sclerosis: A United States clinical testing lab experience

Published:2012-01-31 Issue:2 Volume:13 Page:217-222
ISSN:1748-2968
Container-title:Amyotrophic Lateral Sclerosis
language:en
Short-container-title:Amyotrophic Lateral Sclerosis

Author:

Brown Jeffrey A.,Min Jionghong,Staropoli John F.,Collin Elisa,Bi Stephen,Feng Xin,Barone Rosemary,Cao Yi,O'malley Lei,Xin Winnie,Mullen Thomas E.,Sims Katherine B.

Publisher

Informa UK Limited

Subject

Clinical Neurology,Neurology,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/17482968.2011.643899

Reference23 articles.

1. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

2. SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations

3. Rats Expressing Human Cytosolic Copper–Zinc Superoxide Dismutase Transgenes with Amyotrophic Lateral Sclerosis: Associated Mutations Develop Motor Neuron Disease

4. Angiogenin loss-of-function mutations in amyotrophic lateral sclerosis

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