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The Simple Chordate Ciona intestinalis Has a Reduced Complement of Genes Associated with Fanconi Anemia

Fanconi anemia (FA) is a human genetic disease characterized by congenital defects, bone marrow failure, and increased cancer risk. FA is associated with mutation in one of 24 genes. The protein products of these genes function cooperatively in the FA pathway to orchestrate the repair of DNA interst...

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Detalhes bibliográficos
Publicado no:Evol Bioinform Online
Main Authors: Stanley, Edward C., Azzinaro, Paul A., Vierra, David A., Howlett, Niall G., Irvine, Steven Q.
Formato: Artigo
Idioma:Inglês
Publicado em: Libertas Academica 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4898443/
https://ncbi.nlm.nih.gov/pubmed/27279728
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4137/EBO.S37920
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