Identification and Characterization of Mutations in FANCL Gene: a Second Case of Fanconi Anemia Belonging to FA-L Complementation Group

Fanconi anemia (FA) is a rare autosomal recessive or X-linked disorder characterized by aplastic anemia, cancer susceptibility and cellular sensitivity to DNA crosslinking agents. Eight FA proteins (FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL and FANCM) and three non-FA proteins (FAAP100, FAAP24...

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Main Authors: Ali, Abdullah Mahmood, Kirby, Michelle, Jansen, Michael, Lach, Francis P., Schulte, Jennifer, Singh, Thiyam Ramsing, Batish, Sat D., Auerbach, Arleen D., Williams, David A., Meetei, Amom Ruhikanta
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2760491/
https://ncbi.nlm.nih.gov/pubmed/19405097
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.21032
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