A case of Williams syndrome with p47-phox-deficient chronic granulomatous disease

Japanese Journal of Clinical Immunology

Volumn 26, Issue 5, 2003, Pages 299-303

  Kabuki, Tomoyuki ^a   Kawai, Toshinao ^a   Kin, Yoshiaki ^a   Joh, Kohsuke ^a   Ohashi, Hirofumi ^a   Kosho, Tomoki ^a   Yachie, Akihiro ^b   Kanegane, Hirokazu ^c   Miyawaki, Toshio ^c   Oh Ishi, Tsutomu ^a  

^a SAITAMA CHILDREN'S MEDICAL CENTER   (Japan)

^b KANAZAWA UNIVERSITY   (Japan)

^c UNIVERSITY OF TOYAMA   (Japan)

Author keywords

Neutrophil cytosol factor 1 gene (NCF1); P41 phox; Williams

Indexed keywords

NEUTROPHIL CYTOSOLIC FACTOR 1; PHOSPHOPROTEIN; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE OXIDASE;

ARTICLE; CASE REPORT; CHRONIC GRANULOMATOUS DISEASE; GENETICS; HUMAN; INFANT; MALE; WILLIAMS BEUREN SYNDROME;

GRANULOMATOUS DISEASE, CHRONIC; HUMANS; INFANT; MALE; NADPH OXIDASE; PHOSPHOPROTEINS; WILLIAMS SYNDROME;

EID: 1542548018     PISSN: 09114300     EISSN: 13497413     Source Type: Journal    
DOI: 10.2177/jsci.26.299     Document Type: Article

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