Author:
Ariga T.,Sakiyama Y.,Tomizawa K.,Imajoh-Ohmi S.,Kanegasaki S.,Matsumoto S.
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Reference17 articles.
1. Ariga T, Igarashi T, Ramesh N, Parad R, Cicardi M, Davis AEIII (1989) Type I C1 inhibitor deficiency with a small messenger RNA resulting from deletion of one exon. J Clin Invest 83:1888–1893
2. Ariga T, Nakanishi M, Tomizawa K, Imajoh-Ohmi S, Kanegasaki S, Sakiyama S, Matsumoto S (1992) Genetic heterogeneity in patients with X-linked recessive chronic granulomatous disease. Pediatr Res 31:516–519
3. Battat L, Francke U (1989) Nsi I RFLP at the X-linked chronic granulomatous disease locus (CYBB). Nucleic Acids Res 17: 3619
4. Bolsher BGJM, Boer M, Klein A, Weening RS, Roos D (1991) Point mutations in the β-subunit of cytochrome b558 leading to X-linked chronic granulomatous disease. Blood 77: 248–287
5. Dinauer MC, Curnutte JT, Rosen H, Orkin SH (1989) A missense mutation in the neutrophil cytochrome b heavy chain in cytochrome-positive X-linked chronic granulomatous disease. J Clin Invest 84:2012–2016
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