Update of the human and mouse Fanconi anemia genes

Fanconi anemia (FA) is a recessively inherited disease manifesting developmental abnormalities, bone marrow failure, and increased risk of malignancies. Whereas FA has been studied for nearly 90 years, only in the last 20 years have increasing numbers of genes been implicated in the pathogenesis ass...

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Bibliographic Details
Published in:Hum Genomics
Main Authors: Dong, Hongbin, Nebert, Daniel W., Bruford, Elspeth A., Thompson, David C., Joenje, Hans, Vasiliou, Vasilis
Format: Artigo
Language:Inglês
Published: BioMed Central 2015
Subjects:
Gene Family Update
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4657327/
https://ncbi.nlm.nih.gov/pubmed/26596371
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40246-015-0054-y
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