Genotype-Phenotype Correlation in Chinese Patients with Spinal and Bulbar Muscular Atrophy-Reference-Cited by-同舟云学术

Genotype-Phenotype Correlation in Chinese Patients with Spinal and Bulbar Muscular Atrophy

Published:2015-03-26 Issue:3 Volume:10 Page:e0122279
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Ni Wang,Chen Sheng,Qiao Kai,Wang Ning,Wu Zhi-Ying

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference31 articles.

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2. A comprehensive endocrine description of Kennedy's disease revealing androgen insensitivity linked to CAG repeat length;S Dejager;J Clin Endocrinol Metab,2002

3. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy;AR La Spada;Nature,1991

4. Rethinking genotype and phenotype correlations in polyglutamine expansion disorders;SE Andrew;Hum Mol Genet,1997

5. Diseases of unstable repeat expansion: mechanisms and common principles;JR Gatchel;Nat Rev Genet,2005

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