Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the hyper-IgM syndrome (HIGM2)

Cell

Volumn 102, Issue 5, 2000, Pages 565-575

  Revy, Patrick ^a   Muto, Taro ^b   Levy, Yves ^c   Geissmann, Frédéric ^a   Plebani, Alessandro ^d   Sanal, Ozden ^e   Catalan, Nadia ^a   Forveille, Monique ^a   Dufourcq Lagelouse, Rémi ^a   Gennery, Andrew ^a   Tezcan, Ilhan ^e   Ersoy, Fugen ^e   Kayserili, Hulya ^f   Ugazio, Alberto G ^d   Brousse, Nicole ^a   Muramatsu, Masamichi ^b   Notarangelo, Luigi D ^d   Kinoshita, Kazuo ^b   Honjo, Tasuku ^b   Fischer, Alain ^a   Durandy, Anne ^a   more..

^a HÔPITAL NECKER ENFANTS MALADES   (France)

^b KYOTO UNIVERSITY   (Japan)

^c Hôpital Cochin ^*  (France)

^d UNIVERSITY OF BRESCIA   (Italy)

^e HACETTEPE UNIVERSITY   (Turkey)

^f ISTANBUL UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

CYTIDINE DEAMINASE; HYPERIMMUNE GLOBULIN; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M;

ANTIBODY RESPONSE; ARTICLE; ENZYME ACTIVATION; GENE EXPRESSION; GENE MUTATION; GERMINAL CENTER; HUMAN; HUMAN CELL; LYMPH NODE HYPERPLASIA; PHENOTYPE; PRIORITY JOURNAL;

RODENTIA;

EID: 0034264851     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0092-8674(00)00079-9     Document Type: Article

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