Cytoplasmic localization of FAC is essential for the correction of a prerepair defect in Fanconi anemia group C cells.

Mutations in the gene defective in Fanconi anemia complementation group C, FAC, are responsible for a subset of Fanconi anemia, a group of autosomal recessive disorders characterized by chromosomal instability, hypersensitivity to cross-linking agents, and cancer susceptibility. Although abnormaliti...

ver descrição completa

Detalhes bibliográficos

Publicado no:	J Clin Invest
Autor principal:	Youssoufian, H
Formato:	Artigo
Idioma:	Inglês
Publicado em:	American Society for Clinical Investigation 1996
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC507273/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8621788/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI118635
Tags:	Adicionar Tag Sem tags, seja o primeiro a adicionar uma tag!