Novel mutations, no detectable mRNA and familial genetic analysis of the Wiskott-Aldrich syndrome protein gene in six Japanese patients with Wiskott- Aldrich syndrome

European Journal of Pediatrics

Volumn 159, Issue 1-2, 2000, Pages 23-30

  Sasahara, Y ^a   Kawai, S ^a   Kumaki, S ^a   Ohashi, Y ^a   Minegishi, M ^a   Tsuchiya, S ^a  

^a TOHOKU UNIVERSITY   (Japan)

Author keywords

Mutations Carriers Bone marrow transplantation; Wiskott Aldrich syndrome; Wiskott Aldrich syndrome protein

Indexed keywords

ADOLESCENT; ALLOGENIC BONE MARROW TRANSPLANTATION; ARTICLE; CHILD; CLINICAL ARTICLE; FAMILY STUDY; GENE MUTATION; GENETIC ANALYSIS; HETEROZYGOTE DETECTION; HUMAN; IMMUNE DEFICIENCY; INFANT; MALE; PRIORITY JOURNAL; PROTEIN ANALYSIS; WISKOTT ALDRICH SYNDROME; X CHROMOSOME LINKED DISORDER;

EID: 0033999642     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004310050005     Document Type: Article

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