A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica-Reference-Cited by-同舟云学术

A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica

Published:2018-05-16 Issue:1 Volume:9 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Estrada Karol,Whelan Christopher W.^ORCID,Zhao Fengmei,Bronson Paola,Handsaker Robert E.^ORCID,Sun Chao,Carulli John P.,Harris Tim,Ransohoff Richard M.^ORCID,McCarroll Steven A.,Day-Williams Aaron G.,Greenberg Benjamin M.,MacArthur Daniel G.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/s41467-018-04332-3.pdf

Reference32 articles.

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2. Lennon, V. A. et al. A serum autoantibody marker of neuromyelitis optica: distinction from multiple sclerosis. Lancet 364, 2106–2112 (2004).

3. Papadopoulos, M. C. & Verkman, A. S. Aquaporin 4 and neuromyelitis optica. Lancet Neurol. 11, 535–544 (2012).

4. Ransohoff, R. M. Illuminating neuromyelitis optica pathogenesis. Proc. Natl. Acad. Sci. USA 109, 1001–1002 (2012).

5. Kim, H. J. et al. Common CYP7A1 promoter polymorphism associated with risk of neuromyelitis optica. Neurobiol. Dis. 37, 349–355 (2010).

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