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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Detalles Bibliográficos
Autores principales: Stanley, Edward C., Azzinaro, Paul A., Vierra, David A., Howlett, Niall G., Irvine, Steven Q.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2016
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898443/
https://www.ncbi.nlm.nih.gov/pubmed/27279728
http://dx.doi.org/10.4137/EBO.S37920

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898443/
https://www.ncbi.nlm.nih.gov/pubmed/27279728
http://dx.doi.org/10.4137/EBO.S37920

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