A 25-kb deletion in the 5' region of the cytochrome b558 heavy chain gene (CYBB) in a patient with X-linked chronic granulomatous disease

Human Genetics

Volumn 99, Issue 4, 1997, Pages 469-473

  Faizunnessa, Nurun Nahar ^a   Tsuchiya, Terumasa ^b,d   Kumatori, Atsushi ^a   Kurozumi, Hiroko ^c,e   Imajoh Ohmi, Shinobu ^b   Kanegasaki, Shiro ^b   Nakamura, Michio ^a  

^a NAGASAKI UNIVERSITY   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

^c KANAGAWA CHILDREN'S MEDICAL CENTER   (Japan)

^d TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

^e Yokohama Minami Kyosai Hospital   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; CYTOCHROME B;

ARTICLE; CASE REPORT; CHILD; CHRONIC GRANULOMATOUS DISEASE; EXON; HETEROZYGOTE; HUMAN; HUMAN CELL; IMMUNOCYTOCHEMISTRY; INTRON; MALE; MOLECULAR GENETICS; MOSAICISM; MOTHER; PHENOTYPE; PRIORITY JOURNAL; PULSED FIELD GEL ELECTROPHORESIS; SOUTHERN BLOTTING; X CHROMOSOME LINKAGE;

CELL LINE, TRANSFORMED; CHILD; CYTOCHROME B GROUP; FEMALE; GRANULOMATOUS DISEASE, CHRONIC; HUMANS; MALE; NADPH OXIDASE; PEDIGREE; SEQUENCE DELETION; X CHROMOSOME;

EID: 0030943268     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050390     Document Type: Article

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