Login / Signup

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
  • healthcare
  • genome wide
  • copy number
  • smoking cessation
  • dna methylation