reference/31879877

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/31879877

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endingPage	35
issn	0002-9297
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pageRange	1127-35
publicationName	American journal of human genetics
startingPage	1127
bibliographicCitation	de Boer M, de Klein A, Hossle JP, Seger R, Corbeel L, Weening RS, Roos D. Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox). Am J Hum Genet. 1992 Nov;51(5):1127–35. PMID: 1415254; PMCID: PMC1682833.
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date	199211
identifier	https://pubmed.ncbi.nlm.nih.gov/1415254 https://pubmed.ncbi.nlm.nih.gov/PMC1682833
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/
title	Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox)
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Total number of triples: 57.