Author:
Nóbrega Clévio,Nascimento-Ferreira Isabel,Onofre Isabel,Albuquerque David,Hirai Hirokazu,Déglon Nicole,de Almeida Luís Pereira
Publisher
Public Library of Science (PLoS)
Reference55 articles.
1. Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patients;L Schols;Human molecular genetics,1995
2. Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features;A Durr;Annals of neurology,1996
3. Analysis of SCA1, DRPLA, MJD, SCA2, and SCA6 CAG repeats in 48 Portuguese ataxia families;I Silveira;American journal of medical genetics,1998
4. A survey of spinocerebellar ataxia in South Brazil - 66 new cases with Machado-Joseph disease, SCA7, SCA8, or unidentified disease-causing mutations;LB Jardim;Journal of neurology,2001
5. Glutamine repeats and neurodegeneration;HY Zoghbi;Annual review of neuroscience,2000
Cited by
107 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献