EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans-Reference-Cited by-同舟云学术

EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans

Published:2012-08-26 Issue:9 Volume:18 Page:1418-1422
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Van Hoecke Annelies,Schoonaert Lies,Lemmens Robin,Timmers Mieke,Staats Kim A,Laird Angela S,Peeters Elke,Philips Thomas,Goris An,Dubois Bénédicte,Andersen Peter M,Al-Chalabi Ammar,Thijs Vincent,Turnley Ann M,van Vught Paul W,Veldink Jan H,Hardiman Orla,Van Den Bosch Ludo,Gonzalez-Perez Paloma,Van Damme Philip,Brown Robert H,van den Berg Leonard H,Robberecht Wim

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/nm.2901.pdf

Reference38 articles.

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2. DeJesus-Hernandez, M. et al. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 72, 245–256 (2011).

3. Renton, A.E. et al. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 72, 257–268 (2011).

4. Penco, S. et al. Phenotypic heterogeneity in a SOD1 G93D Italian ALS family: an example of human model to study a complex disease. J. Mol. Neurosci. 44, 25–30 (2011).

5. Kim, W. et al. Anticipation and phenotypic heterogeneity in Korean familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutation. J. Clin. Neurol. 3, 38–44 (2007).

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