Unique and recurrent WAS gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia

Blood Cells, Molecules, and Diseases

Volumn 25, Issue 3-4, 1999, Pages 218-226

  Thompson, L J ^a   Lalloz, M R A ^a   Layton, D M ^a  

^a KING S COLLEGE HOSPITAL   (United Kingdom)

Author keywords

CpG; Mutation; Polymorphism; Prenatal diagnosis; Wiskott Aldrich syndrome; X linked disease; X linked thrombocytopenia

Indexed keywords

ALLELISM; ARTICLE; CLINICAL ARTICLE; DNA SEQUENCE; EXON; FEMALE; GENE CLUSTER; GENE FREQUENCY; GENE LOCATION; GENE LOCUS; GENE MUTATION; HETEROZYGOTE DETECTION; HUMAN; MALE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; THROMBOCYTOPENIA; WISKOTT ALDRICH SYNDROME; X CHROMOSOME LINKED DISORDER;

EID: 0032751887     PISSN: 10799796     EISSN: None     Source Type: Journal    
DOI: 10.1006/bcmd.1999.0247     Document Type: Article

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