The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype study in different populations

BACKGROUND: Analysis of the chromosomal background upon which a mutation occurs can be used to reconstruct the origins of specific disease-causing mutations. The relatively common BRCA1 mutation, 1135insA, has been previously identified as a Norwegian founder mutation. We performed haplotype analysi...

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Detalles Bibliográficos
Autores principales: Rudkin, Teresa M, Hamel, Nancy, Galvez, Maria, Hogervorst, Frans, Gille, Johan JP, Møller, Pål, Apold, Jaran, Foulkes, William D
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1403746/
https://www.ncbi.nlm.nih.gov/pubmed/16509964
http://dx.doi.org/10.1186/1471-2350-7-15

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1403746/
https://www.ncbi.nlm.nih.gov/pubmed/16509964
http://dx.doi.org/10.1186/1471-2350-7-15

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