A novel mutation in intron K of the PROS1 gene causes aberrant RNA splicing and is a common cause of protein S deficiency in a UK thrombophilia cohort |
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Authors: | NJ Beauchamp ME Daly M Makris FE Preston IR Peake |
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Affiliation: | Division of Molecular and Genetic Medicine, Royal Hallamshire Hospital, Sheffield, UK. n.j.beauchamp@sheffield.ac.uk |
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