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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...

詳細記述

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書誌詳細
出版年:Hum Genomics
主要な著者: Dong, Hongbin, Nebert, Daniel W., Bruford, Elspeth A., Thompson, David C., Joenje, Hans, Vasiliou, Vasilis
フォーマット: Artigo
言語:Inglês
出版事項: BioMed Central 2015
主題:
オンライン・アクセス: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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