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

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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Bibliographic Details
Main Authors: Rajashree S Nandagopalan, Shubha R Phadke, Ashwin B Dalal, Prajnya Ranganath
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2014-01-01
Series:Indian Journal of Medical Research
Subjects:
CACP syndrome - Indian cases - novel mutations - PRG4 gene
Online Access:http://www.ijmr.org.in/article.asp?issn=0971-5916;year=2014;volume=140;issue=2;spage=221;epage=226;aulast=Nandagopalan

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http://www.ijmr.org.in/article.asp?issn=0971-5916;year=2014;volume=140;issue=2;spage=221;epage=226;aulast=Nandagopalan

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