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Article

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

Nature genetics - 1 Nov 1999

Marcelino J, Carpten J D, Suwairi W M, Gutierrez O M, Schwartz S, Robbins C, Sood R, Makalowska I, Baxevanis A, Johnstone B, Laxer R M, Zemel L, Kim C A, Herd J K, Ihle J, Williams C, Johnson M, Raman V, Alonso L G, Brunoni D, Gerstein A, Papadopoulos N, Bahabri S A, Trent J M, Warman M L

Abstract excerpt

Altered growth and function of synoviocytes, the intimal cells which line joint cavities and tendon sheaths, occur in a number of skeletal diseases. Hyperplasia of synoviocytes is found in both rheumatoid arthritis and osteoarthritis, despite differences in the underlying aetiologies of the two d...

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PMID: 10545950
DOI: 10.1038/15496

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-10545950-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome.PMID 10545950Read ↗

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The camptodactyly-arthropathy-coxa vara-pericarditis syndrome: Clinical features and genetic mapping to human chromosome 1Semantic proximity Read ↗

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A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataract.Semantic proximity Read ↗

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