Carregant...

An identical novel mutation in BRCA1 and a common haplotype in familial ovarian cancer in non-Ashkenazi Jews.

Unique germline mutations in BRCA1 and BRCA2 account for inherited predisposition to breast and ovarian cancer in high-risk families. In Jewish high-risk individuals of Ashkenazi (east European) descent, three predominant mutations, 185delAG and 5382insC (BRCA1) and 6174delT (BRCA2), seem to account...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Theodor, L., Bar-Sade, R., Kruglikova, A., Ben-Baruch, G., Risel, S., Shiri-Sverdlov, R., Hirsh Yechezkel, G., Modan, B., Papa, M. Z., Rechavi, G., Friedman, E.
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group 1998
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2150352/
https://ncbi.nlm.nih.gov/pubmed/9667663
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!