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A novel mutation in the proteoglycan 4 gene causing CACP syndrome: two sisters report.

İlknur BağrulSerdar CeylanerYasemin Tasci YildizSerife TuncezElif Arslanoglu AydinEsra BağlanSemanur OzdelMehmet Bülbül
Published in: Pediatric rheumatology online journal (2023)
Our report expands the knowledge of PRG4 mutations, which will aid in CACP patient counseling.
Keyphrases
  • case report
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