Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes

American Journal of Human Genetics

Volumn 71, Issue 1, 2002, Pages 198-203

  Feldmann, Jérôme ^a   Prieur, Anne Marie ^b   Quartier, Pierre ^b   Berquin, Patrick ^c   Certain, Stéphanie ^a   Cortis, Elisabetta ^d   Teillac Harnel, Dominique ^e   Fischer, Alain ^a,b   De Saint Basile, Geneviève ^a  

^a INSERM   (France)

^b Service d'immunologie hématologie pédiatrique HÔpital Necker   (France)

^c Section of Radiology   (France)

^d Ospidale Pediatrico Bambino Gesu   (France)

^e HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; RNA;

ARTHRALGIA; ARTICLE; CARTILAGE CELL; CINCA SYNDROME; CLINICAL ARTICLE; GENE MUTATION; HUMAN; INFANT DISEASE; INFLAMMATION; INFLAMMATORY DISEASE; MENINGITIS; MISSENSE MUTATION; NEUROLOGIC DISEASE; NEWBORN; NUCLEOTIDE SEQUENCE; PEDIGREE ANALYSIS; POLYMORPHONUCLEAR CELL; PRIORITY JOURNAL; RASH; SYNDROME DELINEATION;

EID: 0036302235     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/341357     Document Type: Article

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