Deletion at ITPR1 Underlies Ataxia in Mice and Spinocerebellar Ataxia 15 in Humans-Reference-Cited by-同舟云学术

Deletion at ITPR1 Underlies Ataxia in Mice and Spinocerebellar Ataxia 15 in Humans

Published:2007-06-22 Issue:6 Volume:3 Page:e108
ISSN:1553-7404
Container-title:PLoS Genetics
language:en
Short-container-title:PLoS Genet

Author:

van de Leemput Joyce,Chandran Jayanth,Knight Melanie A,Holtzclaw Lynne A,Scholz Sonja,Cookson Mark R,Houlden Henry,Gwinn-Hardy Katrina,Fung Hon-Chung,Lin Xian,Hernandez Dena,Simon-Sanchez Javier,Wood Nick W,Giunti Paola,Rafferty Ian,Hardy John,Storey Elsdon,Gardner R. J. McKinlay,Forrest Susan M,Fisher Elizabeth M. C,Russell James T,Cai Huaibin,Singleton Andrew B

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics (clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

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2. Spinocerebellar ataxia type 15 (SCA15) maps to 3p24.2–3pter: Exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutant.;Neurobiol Dis,2003

3. Discovery genetics: Serendipity in basic research.;ILAR J,2005

4. Ataxia and epileptic seizures in mice lacking type 1 inositol 1,4,5-trisphosphate receptor.;Nature,1996

5. A new autosomal dominant pure cerebellar ataxia.;Neurology,2001

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