(Q73664041)
Statements
Genetic studies of three Japanese patients with p22-phox-deficient chronic granulomatous disease: detection of a possible common mutant CYBA allele in Japan and a genotype-phenotype correlation in these patients (English)
M Yamada
T Ariga
N Kawamura
M Ohtsu
S Imajoh-Ohmi
E Ohshika
O Tatsuzawa
K Kobayashi