Author:
Velasco-Sánchez Daniel,Aracil Asuncion,Montero Raquel,Mas Ana,Jiménez Lorenzo,O’Callaghan Mar,Tondo Maria,Capdevila Antoni,Blanch Josep,Artuch Rafael,Pineda Mercedes
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Reference43 articles.
1. Chamberlain S, Shaw J, Rowland A, Wallis J, South S, Nakamura Y, et al. Mapping of mutation causing Friedreich’s ataxia to human chromosome 9. Nature. 1988;334(6179):248–50.
2. Campuzano V, Montermini L, Molto MD, Pianese L, Cossee M, Cavalcanti F, et al. Friedreich’s ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science. 1996;271(5254):1423–7.
3. Opal P, Y Zoghbi H, Cruse RP. Friedreich ataxia (monograph on the Internet). Uptodate. 2008. Available at: www.uptodate.com . Accessed 21 April 2008
4. Pandolfo M. Friedreich ataxia. Semin Pediatr Neurol. 2003;10(3):163–72.
5. Dutka DP, Donnelly JE, Nihoyannopoulos P, Oakley CM, Nunez DJ. Marked variation in the cardiomyopathy associated with Friedreich’s ataxia. Heart. 1999;81(2):141–7.
Cited by
135 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