A case of Wiskott-Aldrich syndrome with dual mutations in exon 10 of the WASP gene: An additional De Novo one-base insertion, which restores frame shift due to an inherent one-base deletion, detected in the major population of the patient's peripheral blood lymphocytes [3]

Blood

Volumn 92, Issue 2, 1998, Pages 699-701

  Ariga, T ^a   Yamada, M ^a   Sakiyama, Y ^a   Tatsuzawa, O ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EXON; GENE MUTATION; HUMAN; LETTER; LYMPHOCYTE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; WISKOTT ALDRICH SYNDROME;

EID: 0032528485     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v92.2.699     Document Type: Letter

References (9)