A Finnish BRCA1 exon 12 4216-2nt A to G splice acceptor site mutation causes aberrant splicing and frameshift, leading to protein truncation (Q47897282)
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scientific article published in January 2000
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A Finnish BRCA1 exon 12 4216-2nt A to G splice acceptor site mutation causes aberrant splicing and frameshift, leading to protein truncation |
scientific article published in January 2000 |
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A Finnish BRCA1 exon 12 4216-2nt A to G splice acceptor site mutation causes aberrant splicing and frameshift, leading to protein truncation (English)
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Hartikainen JM
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Pirskanen MM
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Arffman AH
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Ristonmaa UK
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Mannermaa AJ
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1 January 2000
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15
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