TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing-Reference-Cited by-同舟云学术

TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing

Published:2010-11-23 Issue:12 Volume:133 Page:3510-3518
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Wang Jun Ling,Yang Xu,Xia Kun,Hu Zheng Mao,Weng Ling,Jin Xin,Jiang Hong,Zhang Peng,Shen Lu,Feng Guo Ji,li Nan,Li Ying Rui,Lei Li Fang,Zhou Jie,Du Juan,Zhou Ya Fang,Pan Qian,Wang Jian,Wang Jun,Li Rui Qiang,Tang Bei Sha

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/133/12/3510/16696928/awq323.pdf

Reference25 articles.

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2. Anti transglutaminase antibodies cause ataxia in mice;Boscolo;PLoS One,2010

3. Genetic diagnosis by whole exome capture and massively parallel DNA sequencing;Choi;Proc Natl Acad Sci USA,2009

4. Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28;Di Bella;Nat Genet,2010

5. Evolution of transglutaminase genes: identification of a transglutaminase gene cluster on human chromosome 15q15. Structure of the gene encoding transglutaminase X and a novel gene family member, transglutaminase Z;Grenard;J Biol Chem,2001

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