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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...
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| 出版年: | Hum Genomics |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2015
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| 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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