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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...

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Dades bibliogràfiques
Publicat a:J Clin Invest
Autor principal: Youssoufian, H
Format: Artigo
Idioma:Inglês
Publicat: American Society for Clinical Investigation 1996
Matèries:
Accés en línia: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
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