Variants in the ALS2 gene are not associated with sporadic amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

Variants in the ALS2 gene are not associated with sporadic amyotrophic lateral sclerosis

Published:2003-05-27 Issue:4 Volume:4 Page:221-222
ISSN:1364-6745
Container-title:Neurogenetics
language:en
Short-container-title:Neurogenetics

Author:

Al-Chalabi Ammar,Hansen Valerie K.,Simpson Claire L.,Xi Jing,Hosler Betsy A.,Powell John F.,McKenna-Yasek Diane,Shaw Christopher E.,Leigh P. Nigel,Brown Robert H.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10048-003-0152-1.pdf

Reference8 articles.

1. Rosen DR, Siddique T, Patterson D, Figlewicz DA, Sapp P, Hentati A, Donaldson D, Goto J, O'Regan JP, Deng HX, et al (1993) Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis (published erratum appears in Nature 1993 364:362). Nature 362:59–62

2. Suthers G, Laing N, Wilton S, Dorosz S, Waddy H (1994) "Sporadic" motoneuron disease due to familial SOD1 mutation with low penetrance. Lancet 344:1773–1773

3. Jackson M, Al-Chalabi A, Enayat ZE, Chioza B, Leigh PN, Morrison KE (1997) Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: analysis of 155 cases and identification of a novel insertion mutation. Ann Neurol 42:803–807

4. Hadano S, Hand CK, Osuga H, Yanagisawa Y, Otomo A, Devon RS, Miyamoto N, Showguchi-Miyata J, Okada Y, Singaraja R, Figlewicz DA, Kwiatkowski T, Hosler BA, Sagie T, Skaug J, Nasir J, Brown RH, Jr., Scherer SW, Rouleau GA, Hayden MR, Ikeda JE (2001) A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2. Nat Genet 29:166–173

5. Yang Y, Hentati A, Deng HX, Dabbagh O, Sasaki T, Hirano M, Hung WY, Ouahchi K, Yan J, Azim AC, Cole N, Gascon G, Yagmour A, Ben Hamida M, Pericak-Vance M, Hentati F, Siddique T (2001) The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis. Nat Genet 29:160–165

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