Sequence variation in the Fanconi anemia gene FAA

Fanconi anemia (FA) is a genetically heterogeneous autosomal recessive syndrome associated with chromosomal instability, hypersensitivity to DNA crosslinking agents, and predisposition to malignancy. The gene for FA complementation group A (FAA) recently has been cloned. The cDNA is predicted to enc...

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Autors principals: Levran, Orna, Erlich, Tamar, Magdalena, Neiva, Gregory, John J., Batish, Sat Dev, Verlander, Peter C., Auerbach, Arleen D.
Format: Artigo
Idioma:Inglês
Publicat: The National Academy of Sciences of the USA 1997
Matèries:
Biological Sciences
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC24261/
https://ncbi.nlm.nih.gov/pubmed/9371798
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