A carregar...

Frataxin point mutations in two patients with Friedreich's ataxia and unusual clinical features

Two patients with a progressive ataxia are presented with clinical features consistent with classic Friedreich's ataxia (FRDA), but also with features unusual for FRDA. Analysis of DNA showed that each patient is heterozygous for the expanded GAA repeat of FRDA, but carries a base change on his...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: McCormack, M., Guttmann, R., Schumann, M., Farmer, J., Stolle, C., Campuzano, V., Koenig, M., Lynch, D.
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2000
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1736939/
https://ncbi.nlm.nih.gov/pubmed/10766903
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.68.5.661
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!