CACP, encoding a secreted proteoglycan, is mutated in camptodactyly- arthropathy-coxa vara-pericarditis syndrome

Nature Genetics

Volumn 23, Issue 3, 1999, Pages 319-322

  Marcelino, Jose ^a   Carpten, John D ^b   Suwairi, Wafaa M ^a,c,d   Gutierrez, Orlando M ^a   Schwartz, Stuart ^a   Robbins, Christiane ^b   Sood, Raman ^b   Makalowska, Izabela ^b   Baxevanis, Andy ^b   Johnstone, Brian ^a   Laxer, Ronald M ^e   Zemel, Lawrence ^f   Kim, Chong Ae ^g   Herd, J Kenneth ^h   Ihle, Johannes ⁱ   Williams, Cal ^j   Johnson, Mark ^j   Raman, Vidya ^j   Alonso, Luís Garcia ^k   Brunoni, Decio ^k   Gerstein, Amy ^l   Papadopoulos, Nickolas ^l   Bahabri, Sultan A ^c   Trent, Jeffrey M ^b   Warman, Matthew L ^a   more..

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^c Riyadh Armed Forces Hospital ^*  (Saudi Arabia)

^d KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER   (Saudi Arabia)

^e HOSPITAL FOR SICK CHILDREN   (Canada)

^f Division of Pediatric Infectious Diseases   (United States)

^g UNIVERSITY OF SÃO PAULO   (Brazil)

^h EAST TENNESSEE STATE UNIVERSITY   (United States)

ⁱ UNIVERSITY HOSPITAL TÜBINGEN   (Germany)

^j WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^k FEDERAL UNIVERSITY OF SÃO PAULO   (Brazil)

^l Howard Hughes Medical Institute   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

HEMOPEXIN; HEPARIN BINDING PROTEIN; MUCIN; PROTEOGLYCAN; SOMATOMEDIN B;

ARTHROPATHY; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CAMPTODACTYLY; COXA VARA; GENE MUTATION; GENETIC CODE; HUMAN; MEGAKARYOCYTE; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PERICARDITIS; PRIORITY JOURNAL; PROTEIN EXPRESSION; SYNDROME; TISSUE DISTRIBUTION;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CATTLE; DNA MUTATIONAL ANALYSIS; FEMALE; GENOTYPE; HUMANS; HYPERPLASIA; JOINT DISEASES; MALE; MOLECULAR SEQUENCE DATA; MUTATION; PERICARDITIS; PHENOTYPE; PROTEOGLYCANS; RNA, MESSENGER; SEQUENCE HOMOLOGY, AMINO ACID; SYNDROME; SYNOVIAL MEMBRANE;

EID: 0032699840     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/15496     Document Type: Article

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