The P413L chromogranin B variation in French patients with sporadic amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

The P413L chromogranin B variation in French patients with sporadic amyotrophic lateral sclerosis

Published:2010-10-11 Issue:3 Volume:12 Page:210-214
ISSN:1748-2968
Container-title:Amyotrophic Lateral Sclerosis
language:en
Short-container-title:Amyotrophic Lateral Sclerosis

Author:

Blasco Hélène,Corcia Philippe,Veyrat-Durebex Charlotte,Coutadeur Cathleen,Fournier Clémentine,Camu William,Gordon Paul,Praline Julien,Andres Christian R.,Vourc'h Patrick,

Publisher

Informa UK Limited

Subject

Neurology (clinical),Neurology,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/17482968.2010.522587

Reference14 articles.

1. Genetics of sporadic ALS

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

3. The Chromogranin–Secretogranin Family

4. Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis

5. Disulfide cross-linked protein represents a significant fraction of ALS-associated Cu, Zn-superoxide dismutase aggregates in spinal cords of model mice

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