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Genetic screening for multiple endocrine neoplasia syndrome type 1 (MEN-1): when and how

Multiple endocrine neoplasia syndrome type 1 (MEN1) syndrome has benefited from the identification of the gene whose mutations account for the genetic susceptibility to develop endocrine tumors. Asymptomatic MEN1 mutant carriers need to be clearly recognized because the gene-related mutations confer...

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Detalles Bibliográficos
Autor principal: Falchetti, Alberto
Formato: Texto
Lenguaje:English
Publicado: Medicine Reports Ltd 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2948394/
https://www.ncbi.nlm.nih.gov/pubmed/20948872
http://dx.doi.org/10.3410/M2-14