Genotype and laboratory and clinical phenotypes of protein S deficiency

American Journal of Clinical Pathology

Volumn 137, Issue 2, 2012, Pages 178-184

  Duebgen, Sebastian ^a   Kauke, Teresa ^a   Marschall, Christoph ^b   Giebl, Andreas ^a   Lison, Susanne ^a   Hart, Christina ^c   Dick, Andrea ^a   Spannagl, Michael ^a  

^a UNIVERSITY OF MUNICH   (Germany)

^b Center for Human Genetics and Laboratory Medicine   (Germany)

^c UNIVERSITY OF REGENSBURG   (Germany)

Author keywords

Genotype; Laboratory assessment; Phenotype; PROS1; Protein S deficiency

Indexed keywords

PROTEIN S;

ANTICOAGULATION; ARTICLE; DEEP VEIN THROMBOSIS; DNA SEQUENCE; GENE DELETION; GENE MUTATION; GENETIC ANALYSIS; GENETIC DISORDER; GENOTYPE; HORMONAL CONTRACEPTION; HUMAN; LABORATORY TEST; MAJOR CLINICAL STUDY; MUTATIONAL ANALYSIS; PHENOTYPE; PREGNANCY; PRIORITY JOURNAL; PROTEIN DETERMINATION; PROTEIN FUNCTION; PROTEIN S DEFICIENCY; SEQUENCE ANALYSIS; THROMBOPHILIA;

BLOOD PROTEINS; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; HUMANS; MUTATION; PROTEIN S DEFICIENCY; THROMBOPHILIA;

EID: 84856404475     PISSN: 00029173     EISSN: 19437722     Source Type: Journal    
DOI: 10.1309/AJCP40UXNBTXGKUX     Document Type: Article

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