A new candidate mutation (N528S) within the von Willebrand factor propeptide identified in a Japanese patient with phenotype IIC of von Willebrand disease

European Journal of Haematology

Volumn 61, Issue 2, 1998, Pages 145-148

  Gaucher, C ^a   Uno, H ^b   Yamazaki, T ^c   Mashiba, H ^e   Mazurier, C ^a,d  

^a Lab de Recherche sur l'Hemostase   (France)

^b Kure Kyosai Hospital   (Japan)

^c NAGOYA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^d LFB   (France)

^e NONE

Author keywords

Phenotype IIC; Von Willebrand's disease; vWF gene; vWF propeptide

Indexed keywords

ARTICLE; BLOOD CLOTTING; CLINICAL ARTICLE; GENE MUTATION; GENETIC SCREENING; HETEROZYGOSITY; HUMAN; NUCLEOTIDE SEQUENCE; PEDIGREE ANALYSIS; PRIORITY JOURNAL; SEQUENCE ANALYSIS; VON WILLEBRAND DISEASE;

EID: 0031831816     PISSN: 09024441     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1600-0609.1998.tb01076.x     Document Type: Article

References (22)

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