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CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 319, doi. 10.1038/15496
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- Publication type:
- Article
Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia.
- Published in:
- Nature Genetics, 1999, v. 23, n. 1, p. 94, doi. 10.1038/12699
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- Publication type:
- Article