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

Thrombosis and Haemostasis

Volumn 79, Issue 6, 1998, Pages 1086-1091

  Beauchamp, N J ^a   Daly, M E ^a   Makris, M ^a   Preston, F E ^a   Peake, I R ^a  

^a ROYAL HALLAMSHIRE HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA; PROTEIN S;

ADOLESCENT; ADULT; AGED; ARTICLE; BINDING SITE; CLINICAL ARTICLE; EXON; FEMALE; GENE MUTATION; GENE SEQUENCE; HAPLOTYPE; HUMAN; INTRON; MALE; PRIORITY JOURNAL; PROTEIN S DEFICIENCY; RNA SPLICING; THROMBOPHILIA; VEIN THROMBOSIS;

EID: 0031832407     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1615020     Document Type: Article

References (15)

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