A carregar...
Progressive External Ophthalmoplegia and Vision and Hearing Loss in a Patient With Mutations in POLG2 and OPA1
OBJECTIVE: To describe the clinical features, muscle pathological characteristics, and molecular studies of a patient with a mutation in the gene encoding the accessory subunit (p55) of polymerase γ (POLG2) and a mutation in the OPA1 gene. DESIGN: Clinical examination and morphological, biochemical,...
Na minha lista:
Main Authors: | , , , , , , , , , , , , |
---|---|
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
2008
|
Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2364721/ https://ncbi.nlm.nih.gov/pubmed/18195150 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/archneurol.2007.9 |
Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|