A Finnish BRCA1 exon 12 4216-2nt A to G splice acceptor site mutation causes aberrant splicing and frameshift, leading to protein truncation |
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Authors: | Hartikainen J M Pirskanen M M Arffman A H Ristonmaa U K Mannermaa A J |
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Affiliation: | Chromosome and DNA laboratory, Kuopio University Hospital, P. O. BOX 1777, FIN-70211 Kuopio, Finland. Jaana.Hartikainen@kuh.fi |
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