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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Publicat a:Evol Bioinform Online
Autors principals: Stanley, Edward C., Azzinaro, Paul A., Vierra, David A., Howlett, Niall G., Irvine, Steven Q.
Format: Artigo
Idioma:Inglês
Publicat: Libertas Academica 2016
Matèries:
Original Research
Accés en línia: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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