Unclassified variants identified inBRCA1exon 11: Consequences on splicing
Author:
Publisher
Wiley
Subject
Cancer Research,Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/gcc.20546/fullpdf
Reference24 articles.
1. Analysis of missense variation in human BRCA1 in the context of interspecific sequence variation;Abkevich;J Med Genet,2004
2. Systematic mRNA analysis for the effect of MLH1 and MSH2 missense and silent mutations on aberrant splicing;Auclair;Hum Mutat,2006
3. NF1 mRNA biogenesis: Effect of the genomic milieu in splicing regulation of the NF1 exon 37 region;Baralle;FEBS Lett,2006
4. BRCA1 in breast and ovarian cancer predisposition;Billack;Cancer Lett,2005
5. Listening to silence and understanding nonsense: Exonic mutations that affect splicing;Cartegni;Nat Rev Genet,2002
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