The expression of 22-kD subunit of cytochrome b558 in patients with X-linked chronic granulomatous disease
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1991.tb00516.x/fullpdf
Reference13 articles.
1. Cloning the gene for an inherited human disorder - chronic granulomatous disease - on the basis of its chromosomal location;Royer-Pokora;Nature,1986
2. The glycoprotein encoded by the chronic granulomatous disease locus is a component of the neutrophil cyto-chrome b complex;Dinauer;Nature,1987
3. The X-linked chronic granulomatous disease gene codes for the chain of cytochrome b-245*;Teahan;Nature,1987
4. Purified cytochrome b from human granulocyte plasma membrane is comprised of two polypeptides with relative molecular weight of 91,000 and 22,000;Parkos;J Clin Invest,1987
5. Absence of both cytochrome b-245 subunits from neutrophils in X-linked chronic granulomatous disease;Segal;Nature,1987
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A 15-base pair (bp) palindromic insertion associated with a 3-bp deletion in exon 10 of the gp91-phox gene, detected in two patients with X-linked chronic granulomatous disease;Human Genetics;1995-07
2. A newly recognized point mutation in the cytochrome b558 heavy chain gene replacing alanine57 by glutamic acid, in a patient with cytochrome b positive X-linked chronic granulomatous disease;European Journal of Pediatrics;1993-06
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