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A newly recognized point mutation in the cytochrome b558heavy chain gene replacing alanine57by glutamic acid, in a patient with cytochrome b positive X-linked chronic granulomatous disease

โœ Scribed by T. Ariga; Y. Sakiyama; K. Tomizawa; S. Imajoh-Ohmi; S. Kanegasaki; S. Matsumoto


Publisher
Springer
Year
1993
Tongue
English
Weight
799 KB
Volume
152
Category
Article
ISSN
0340-6997

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Two novel point mutations in the gp91-phox gene of two Japanese with X-linked chronic granulomatous disease were identified by sequence analysis of polymerase chain reaction amplified DNA fragments