CARD15 mutations in Blau syndrome

Nature Genetics

Volumn 29, Issue 1, 2001, Pages 19-20

  Miceli Richard, Corinne ^a   Lesage, Suzanne ^a   Rybojad, Michel ^b   Prieur, Anne Marie ^c   Manouvrier Hanu, Sylvie ^d   Häfner, Renate ^e   Chamaillard, Mathias ^a,f   Zouali, Habib ^a   Thomas, Gilles ^a,f   Hugot, Jean Pierre ^a,b  

^a FONDATION JEAN DAUSSET CEPH   (France)

^b HÔPITAL ROBERT DEBRÉ   (France)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

^d LILLE UNIVERSITY HOSPITAL   (France)

^e Rheumatic Children's Hospital   (Germany)

^f INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CASPASE RECRUITMENT DOMAIN PROTEIN 15; NUCLEOTIDE BINDING PROTEIN; UNCLASSIFIED DRUG;

ARTHRITIS; ARTICLE; BLAU SYNDROME; CAMPTODACTYLY; COLON CROHN DISEASE; CONTROLLED STUDY; FAMILY; FRANCE; GENE MUTATION; GENETIC SUSCEPTIBILITY; GERMANY; GRANULOMATOSIS; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RASH; UVEITIS;

ARTHRITIS; CARRIER PROTEINS; EXANTHEMA; FEMALE; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; JOINT DISEASES; MALE; MUTATION; NOD2 SIGNALING ADAPTOR PROTEIN; PEDIGREE; SYNDROME; UVEITIS;

EID: 17944372335     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng720     Document Type: Article

References (9)