Molecular study of VWF gene from Mexican Mestizo patients with von Willebrand disease, and the finding of three new mutations

Blood Cells, Molecules, and Diseases

Volumn 39, Issue 3, 2007, Pages 361-365

  Melo Nava, Brenda M ^a   Benítez, Herminia ^b   Palacios, J Jorge ^a   Nieva, Beatriz ^b   Arenas, Diego ^a   Jaloma Cruz, A Rebeca ^c   Navarrete, Carmen ^a   Salamanca, Fabio ^a   Peñaloza, Rosenda ^a  

^a INSTITUTO MEXICANO DEL SEGURO SOCIAL   (Mexico)

^b HOSPITAL DE PEDIATRÍA   (Mexico)

^c CENTRO DE INVESTIGACIÓN BIOMÉDICA DE OCCIDENTE   (Mexico)

Author keywords

Mexican population; New mutations; von Willebrand disease

Indexed keywords

VON WILLEBRAND FACTOR;

ADOLESCENT; AFRICA; ALLELE; ARTICLE; CAUCASIAN; CHILD; CLINICAL ARTICLE; EXON; FEMALE; GENE AMPLIFICATION; GENE MUTATION; GENE SEQUENCE; HUMAN; HUMAN TISSUE; INDIGENOUS PEOPLE; MALE; MOLECULAR GENETICS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; VON WILLEBRAND DISEASE;

ADOLESCENT; ALLELES; CHILD; CHILD, PRESCHOOL; EXONS; FEMALE; HUMANS; MALE; MEXICO; MUTATION, MISSENSE; VON WILLEBRAND DISEASE; VON WILLEBRAND FACTOR;

EID: 34748881191     PISSN: 10799796     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bcmd.2007.06.007     Document Type: Article

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