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January 24, 2023Pediatric Rheumatology9 citationsOpen Access

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

İBİlknur BağrulSCSerdar CeylanerYYYasemin Taşçı Yıldız

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Abstract

Our report expands the knowledge of PRG4 mutations, which will aid in CACP patient counseling.

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Cite This Study

Bağrul et al. (2023) studied this question.

synapsesocial.com/papers/69df06b858b92af24d7a0d41https://doi.org/10.1186/s12969-023-00793-z
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