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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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| Autori principali: | , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2006
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1403746/ https://ncbi.nlm.nih.gov/pubmed/16509964 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-7-15 |
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