Homozygosity analysis in amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

Homozygosity analysis in amyotrophic lateral sclerosis

Published:2013-04-24 Issue:12 Volume:21 Page:1429-1435
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Mok Kin,Laaksovirta Hannu,Tienari Pentti J,Peuralinna Terhi,Myllykangas Liisa,Chiò Adriano,Traynor Bryan J,Nalls Michael A,Gurunlian Nicole,Shatunov Aleksey,Restagno Gabriella,Mora Gabriele,Nigel Leigh P,Shaw Chris E,Morrison Karen E,Shaw Pamela J,Al-Chalabi Ammar,Hardy John,Orrell Richard W

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg201359.pdf

Reference39 articles.

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2. Rosen DR, Siddique T, Patterson D et al: Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 1993; 362: 59–62, (Erratum in: Nature; 364: 362).

3. Sreedharan J, Blair IP, Tripathi VB et al: TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science 2008; 319: 1668–1672.

4. Vance C, Rogelj B, Hortobágyi T et al: Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science 2009; 323: 1208–1211.

5. Johnson JO, Mandrioli J, Benatar M et al: Exome sequencing reveals VCP mutations as a cause of familial ALS. Neuron 2010; 68: 857–864, (Erratum in: Neuron 2011;69:397).

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