Autosomal recessive chronic granulomatous disease caused by defects in NCF-1, the gene encoding the phagocyte p47-phox: mutations not arising in the NCF-1 pseudogenes.
PubMed Identifier: 11133775
author list: Noack D, Rae J, Cross AR, Ellis BA, Newburger PE, Curnutte JT, Heyworth PG
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published in: Blood
has major subject area list: Granulomatous Disease, Chronic; Mutation; Phosphoproteins
has minor subject area list: Adolescent; Adult; Alleles; Child; Child, Preschool; DNA Mutational Analysis; Exons; Family Health; Female; Genotype; Humans; Male; NADPH Oxidases; Polymerase Chain Reaction; Pseudogenes
information resource reference: Noack D, Rae J, Cross AR, Ellis BA, Newburger PE, Curnutte JT, Heyworth PG. Autosomal recessive chronic granulomatous disease caused by defects in NCF-1, the gene encoding the phagocyte p47-phox: mutations not arising in the NCF-1 pseudogenes. Blood. 2001 Jan 01; 97(1):305-11.
journal title abbreviation: Blood
publication date: 2001-01-01T00:00:00
year: 2001
type: Academic Article
type: Article
type: Document
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has subject area: Granulomatous Disease, Chronic
has subject area: Mutation
has subject area: Phosphoproteins
has subject area: Adolescent
has subject area: Adult
has subject area: Alleles
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has subject area: Child, Preschool
has subject area: DNA Mutational Analysis
has subject area: Exons
has subject area: Family Health
has subject area: Female
has subject area: Genotype
has subject area: Humans
has subject area: Male
has subject area: NADPH Oxidases
has subject area: Polymerase Chain Reaction
has subject area: Pseudogenes
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linked information resource: Autosomal recessive chronic granulomatous disease caused by defects in NCF-1, the gene encoding the phagocyte p47-phox: mutations not arising in the NCF-1 pseudogenes.

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