A novel mutation in the proteoglycan 4 gene causing CACP syndrome: two sisters report.
İlknur BağrulSerdar CeylanerYasemin Tasci YildizSerife TuncezElif Arslanoglu AydinEsra BağlanSemanur OzdelMehmet BülbülPublished in: Pediatric rheumatology online journal (2023)
Our report expands the knowledge of PRG4 mutations, which will aid in CACP patient counseling.