Combined protein C and protein S deficiency in a family with repetitive thromboembolism and segregated gene mutations

Internal Medicine

Volumn 42, Issue 3, 2003, Pages 268-272

  Hayashida, Mie ^c   Yamada, Hiroyoshi ^c   Yamazaki, Satoshi ^c   Nomura, Hiroshi ^c   Yoshimura, Kazuhiko ^c   Kitahara, Osamu ^c   Momose, Kunio ^c   Kubo, Keishi ^a   Kurihara, Masako ^b   Hamasaki, Naotaka ^b  

^a SHINSHU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b KYUSHU UNIVERSITY HOSPITAL   (Japan)

^c Omachi General Hospital   (Japan)

Author keywords

Combined deficiency; Genetic analysis; Protein C; Protein S; Venous thrombosis

Indexed keywords

DNA; HEPARIN; PROTEIN C; PROTEIN S; UROKINASE; WARFARIN;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; COMORBIDITY; COMPUTER ASSISTED TOMOGRAPHY; DEEP VEIN THROMBOSIS; DNA SEQUENCE; FAMILY; GENE MUTATION; GENETIC ANALYSIS; GENOTYPE PHENOTYPE CORRELATION; HUMAN; INFERIOR CAVA VEIN OBSTRUCTION; INTRAVASCULAR ULTRASOUND; JAPAN; LEG PHLEBOGRAPHY; LEG THROMBOSIS; MOLECULAR GENETICS; NUCLEAR MAGNETIC RESONANCE IMAGING; POLYMERASE CHAIN REACTION; PROTEIN C DEFICIENCY; PROTEIN S DEFICIENCY; THROMBOEMBOLISM;

EID: 0242417042     PISSN: 09182918     EISSN: None     Source Type: Journal    
DOI: 10.2169/internalmedicine.42.268     Document Type: Article

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