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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Bibliografiska uppgifter
I publikationen:Hum Genomics
Huvudupphovsmän: Dong, Hongbin, Nebert, Daniel W., Bruford, Elspeth A., Thompson, David C., Joenje, Hans, Vasiliou, Vasilis
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2015
Ämnen:
Gene Family Update
Länkar: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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