Novel mutations in PRG4 gene in two Indian families with camptodactyly-arthropathy- coxa vara- pericarditis (CACP) syndrome

BACKGROUND & OBJECTIVES: Camptodactyly – arthropathy- coxa vara- pericarditis (CACP) syndrome is an autosomal recessive disorder caused by mutations in the PRG4 (proteoglycan 4) gene. Hallmarks of the syndrome include congenital or early-onset camptodactyly and arthropathy with synovial hyperpla...

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Detalles Bibliográficos
Autores principales: Nandagopalan, Rajashree S., Phadke, Shubha R., Dalal, Ashwin B., Ranganath, Prajnya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4216495/
https://www.ncbi.nlm.nih.gov/pubmed/25297354

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4216495/
https://www.ncbi.nlm.nih.gov/pubmed/25297354

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