Mutational analysis of patients with p47-phox-deficient chronic granulomatous disease: The significance of recombination events between the p47-phox gene (NCF1) and its highly homologous pseudogenes

Experimental Hematology

Volumn 29, Issue 2, 2001, Pages 234-243

  Vázquez, Nancy ^a   Lehrnbecher, Thomas ^a   Chen, Renee ^a   Christensen, Barbara L ^a   Gallin, John I ^b   Malech, Harry ^b   Holland, Steven ^b   Zhu, Shaoxian ^a   Chanock, Stephen J ^a  

^a NATIONAL CANCER INSTITUTE   (United States)

^b NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES   (United States)

Author keywords

Allele; Genetics; Immunodeficiency; Nicotinamide adenine dinucleotide phosphate oxidase; Phagocyte

Indexed keywords

NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE;

ALLELE; ARTICLE; CLINICAL ARTICLE; EXON; GENE CONVERSION; GENE DELETION; GENE MUTATION; GENETIC RECOMBINATION; GRANULOMATOSIS; HUMAN; HUMAN CELL; PRIORITY JOURNAL; PSEUDOGENE; SEQUENCE ANALYSIS;

BASE SEQUENCE; BLOTTING, NORTHERN; DNA MUTATIONAL ANALYSIS; DNA RESTRICTION ENZYMES; EXONS; GENE DELETION; GRANULOMATOUS DISEASE, CHRONIC; HUMANS; INTRONS; MUTATION; NADPH OXIDASE; PHAGOCYTES; PHOSPHOPROTEINS; POLYMERASE CHAIN REACTION; PSEUDOGENES; RECOMBINATION, GENETIC; RNA; RNA, MESSENGER; SEQUENCE ANALYSIS, DNA;

EID: 0035141062     PISSN: 0301472X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0301-472X(00)00646-9     Document Type: Article

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