Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia-Reference-Cited by-同舟云学术

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia

Published:2011-08-21 Issue:7363 Volume:477 Page:211-215
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Deng Han-Xiang,Chen Wenjie,Hong Seong-Tshool,Boycott Kym M.,Gorrie George H.,Siddique Nailah,Yang Yi,Fecto Faisal,Shi Yong,Zhai Hong,Jiang Hujun,Hirano Makito,Rampersaud Evadnie,Jansen Gerard H.,Donkervoort Sandra,Bigio Eileen H.,Brooks Benjamin R.,Ajroud Kaouther,Sufit Robert L.,Haines Jonathan L.,Mugnaini Enrico,Pericak-Vance Margaret A.,Siddique Teepu

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/nature10353.pdf

Reference36 articles.

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3. Kabashi, E. et al. TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis. Nature Genet. 40, 572–574 (2008)

4. Sreedharan, J. et al. TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science 319, 1668–1672 (2008)

5. Kwiatkowski, T. J., Jr et al. Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science 323, 1205–1208 (2009)

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