First report of clinical, functional, and molecular investigation of chronic granulomatous disease in nine Jordanian families

Journal of Clinical Immunology

Volumn 29, Issue 2, 2009, Pages 215-230

  Bakri, Faris G ^b   Martel, Cécile ^a   Khuri Bulos, Najwa ^b   Mahafzah, Azmi ^b   El Khateeb, Mohammad S ^c,f   Al Wahadneh, Adel M ^d   Hayajneh, Wail A ^e   Hamamy, Hanan A ^f   Maquet, Elisabeth ^a   Molin, Michelle ^a   Stasia, Marie José ^a,g  

^a LABORATOIRE TIMC IMAG   (France)

^b JORDAN UNIVERSITY HOSPITAL   (Jordan)

^c UNIVERSITY OF JORDAN   (Jordan)

^d KING HUSSEIN MEDICAL CENTER   (Jordan)

^e JORDAN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Jordan)

^f National Center for Diabetes Endocrinology and Genetics Jordan   (Jordan)

^g GRENOBLE UNIVERSITY HOSPITAL   (France)

Author keywords

Autosomal recessive; Chronic granulomatous disease; CYBA; CYBB; Innate immunodeficiency; NADPH oxidase; NCF1; NCF2; X linked recessive

Indexed keywords

PROTEIN P22; PROTEIN P47; PROTEIN P67;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHILD; CHRONIC GRANULOMATOUS DISEASE; CLINICAL ARTICLE; CONSANGUINEOUS MARRIAGE; CONTROLLED STUDY; CYBA GENE; FEMALE; GENE; GENE FREQUENCY; GENETIC HETEROGENEITY; HUMAN; INFANT; JORDAN; MALE; MISSENSE MUTATION; NCF1 GENE; NCF2 GENE; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; CHILD; CHILD, PRESCHOOL; FEMALE; GENOTYPE; GRANULOMATOUS DISEASE, CHRONIC; HUMANS; JORDAN; LEUKOCYTES, MONONUCLEAR; MALE; MEMBRANE GLYCOPROTEINS; MOLECULAR SEQUENCE DATA; MUTATION; NADPH OXIDASE; NEUTROPHILS; YOUNG ADULT;

EID: 61849102269     PISSN: 02719142     EISSN: 15732592     Source Type: Journal    
DOI: 10.1007/s10875-008-9243-y     Document Type: Article

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