Mutation Analysis of the BRCA1 and BRCA2 Genes in the Belgian Patient Population and Identification of a Belgian Founder Mutation BRCA1 IVS5+3A>G

Since the identification of the BRCA1 and BRCA2 genes, several hundred different germline mutations in both genes have been reported. Recurrent mutations are rare and mainly due to founder effects. As the mutational spectrum of the BRCA1 and BRCA2 genes in the Belgian patient population is largely u...

Descripción completa

Detalles Bibliográficos
Autores principales: Claes, Kathleen, Machackova, Eva, De Vos, Michel, Poppe, Bruce, De Paepe, Anne, Messiaen, Ludwine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 1999
Materias:
Other
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3851655/
https://www.ncbi.nlm.nih.gov/pubmed/10595255
http://dx.doi.org/10.1155/1999/241046

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3851655/
https://www.ncbi.nlm.nih.gov/pubmed/10595255
http://dx.doi.org/10.1155/1999/241046

Ejemplares similares