Poor relationship between phenotypes of protein S deficiency and mutations in the protein S alpha gene

Thrombosis and Haemostasis

Volumn 82, Issue 6, 1999, Pages 1634-1638

  Hermida, José ^a   Faioni, Elena M ^a,b   Mannucci, Pier Mannuccio ^a  

^a UNIVERSITY OF MILAN   (Italy)

^b Hemophilia and Thrombosis Center   (Italy)

Author keywords

Mutations; Phenotype; Protein S Heerlen; Protein S gene

Indexed keywords

PROTEIN S;

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DEEP VEIN THROMBOSIS; EXON; GENE MUTATION; GENOTYPE; HUMAN; INTRON; MISSENSE MUTATION; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN S DEFICIENCY; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0032700739     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1614891     Document Type: Article

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