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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Detalles Bibliográficos
Autores principales: Dong, Hongbin, Nebert, Daniel W., Bruford, Elspeth A., Thompson, David C., Joenje, Hans, Vasiliou, Vasilis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Gene Family Update
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4657327/
https://www.ncbi.nlm.nih.gov/pubmed/26596371
http://dx.doi.org/10.1186/s40246-015-0054-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4657327/
https://www.ncbi.nlm.nih.gov/pubmed/26596371
http://dx.doi.org/10.1186/s40246-015-0054-y

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