Characterization of 11 novel mutations in the X-linked chronic granulomatous disease (CYBB gene).

Human mutation

Volumn 18, Issue 2, 2001, Pages 163-

  Gerard B ^a   El Benna, J ^a   Alcain, F ^a   Gougerot Pocidalo, M A ^a   Grandchamp, B ^a   Chollet Martin, S ^a  

^a BICHAT HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CYBB PROTEIN, HUMAN; CYTOCHROME B; CYTOCHROME B558; MEMBRANE PROTEIN; REACTIVE OXYGEN METABOLITE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE OXIDASE;

ARTICLE; CHRONIC GRANULOMATOUS DISEASE; FEMALE; GENE DELETION; GENETIC LINKAGE; GENETICS; HETEROZYGOTE; HUMAN; MALE; METABOLISM; MUTATION; NEUTROPHIL; NUCLEOTIDE SEQUENCE; SINGLE STRAND CONFORMATION POLYMORPHISM; X CHROMOSOME;

CYTOCHROME B GROUP; DNA MUTATIONAL ANALYSIS; FEMALE; GRANULOMATOUS DISEASE, CHRONIC; HETEROZYGOTE; HUMANS; LINKAGE (GENETICS); MALE; MEMBRANE GLYCOPROTEINS; MUTATION; NADPH OXIDASE; NEUTROPHILS; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; REACTIVE OXYGEN SPECIES; SEQUENCE DELETION; X CHROMOSOME;

MLCS; MLOWN;

EID: 0035432944     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.1166     Document Type: Article

References (0)