Familial ALS with extreme phenotypic variability due to the I113T SOD1 mutation-Reference-Cited by-同舟云学术

Familial ALS with extreme phenotypic variability due to the I113T SOD1 mutation

Published:2010-01 Issue:1-2 Volume:11 Page:232-236
ISSN:1748-2968
Container-title:Amyotrophic Lateral Sclerosis
language:en
Short-container-title:Amyotrophic Lateral Sclerosis

Author:

Lopate Glenn,Baloh Robert H.,Al-Lozi Muhammad T.,Miller Timothy M.,Fernandes Filho J. Americo,Ni Oliver,Leston Alison,Florence Julaine,Schierbecker Jeanine,Allred Peggy

Publisher

Informa UK Limited

Subject

Clinical Neurology,Neurology,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/17482960902898069

Reference15 articles.

1. Cognitive impairment in amyotrophic lateral sclerosis

2. Epidemiology of mutations in superoxide dismutase in amyotrophic lateal sclerosis

3. SOD1 gene mutations in ALS patients from British Columbia, Canada: Clinical features, neurophysiology and ethical issues in management

4. Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients.

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