Mutations of the Fanconi anemia group A gene (FAA) in Italian patients.

Fanconi anemia (FA) is an autosomal recessive disease characterized by progressive pancytopenia, congenital malformations, and predisposition to acute myeloid leukemia. At least five complementation groups (FA-A-FA-E) have been identified. The relative prevalence of FA-A has been estimated at an ave...

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Detalhes bibliográficos
Main Authors: Savino, M, Ianzano, L, Strippoli, P, Ramenghi, U, Arslanian, A, Bagnara, G P, Joenje, H, Zelante, L, Savoia, A
Formato: Artigo
Idioma:Inglês
Publicado em: 1997
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1716093/
https://ncbi.nlm.nih.gov/pubmed/9399890
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