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variants BRCA1 IVS6-1G>A and BRCA2 IVS15+1G>A lead to aberrant splicing of the transcripts

variants BRCA1 IVS6-1G>A and BRCA2 IVS15+1G>A lead to aberrant splicing of the transcripts

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_67584448

variants BRCA1 IVS6-1G>A and BRCA2 IVS15+1G>A lead to aberrant splicing of the transcripts

About this item

Full title

variants BRCA1 IVS6-1G>A and BRCA2 IVS15+1G>A lead to aberrant splicing of the transcripts

Publisher

Boston: Boston : Springer US

Journal title

Breast cancer research and treatment, 2009-09, Vol.117 (2), p.461-465

Language

English

Formats

Publication information

Publisher

Boston: Boston : Springer US

More information

Scope and Contents

Contents

The majority of BRCA1 and BRCA2 deleterious mutations and variants of unknown significance have been identified in genomic DNA and their effects at the mRNA level have not been reported. Our aim was to ascertain the pathological effect of the BRCA1 IVS6-1G>A (c. 302-1G>A) and the BRCA2 IVS15+1G>A (c. 7617+1G>A) variants detected in Spanish breast/o...

Alternative Titles

Full title

variants BRCA1 IVS6-1G>A and BRCA2 IVS15+1G>A lead to aberrant splicing of the transcripts

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_67584448

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_67584448

Other Identifiers

ISSN

0167-6806

E-ISSN

1573-7217

DOI

10.1007/s10549-008-0154-7

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