Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndrome

Clinical Immunology

Volumn 97, Issue 3, 2000, Pages 203-210

  Minegishi, Yoshiyuki ^a   Lavoie, Aubert ^b   Cunningham Rundles, Charlotte ^c   Bédard, Pierre Michel ^b   Hébert, Jacques ^b   Côté, Louise ^b   Dan, Kazuo ^d   Sedlak, Debra ^e   Buckley, Rebecca H ^e   Fischer, Alain ^f   Durandy, Anne ^f   Conley, Mary Ellen ^a,g  

^a ST JUDE CHILDREN S RESEARCH HOSPITAL   (United States)

^b UNIVERSITÉ LAVAL   (Canada)

^c MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^d NIPPON MEDICAL SCHOOL   (Japan)

^e DUKE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^f HÔPITAL NECKER ENFANTS MALADES   (France)

^g UNIVERSITY OF TENNESSEE COLLEGE OF MEDICINE   (United States)

Author keywords

B cells; Class switch recombination; IgM; Immunodeficiency; Lymphoid hyperplasia; RNA editing; Somatic mutation

Indexed keywords

CD40 ANTIGEN; CYTIDINE DEAMINASE; HEMAGGLUTININ; IMMUNOGLOBULIN M;

ADOLESCENT; ADULT; ANEMIA; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; B LYMPHOCYTE; CANADA; CASE REPORT; CHILD; ENZYME ACTIVATION; FEMALE; GENE MUTATION; HUMAN; HYPERIMMUNOGLOBULINEMIA; IMMUNE DEFICIENCY; JAPAN; LYMPHOID HYPERPLASIA; MALE; PRIORITY JOURNAL; RNA EDITING; SEQUENCE HOMOLOGY; SYNDROME;

EID: 0033669973     PISSN: 15216616     EISSN: None     Source Type: Journal    
DOI: 10.1006/clim.2000.4956     Document Type: Article

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