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Functional analysis of 22 splice-site mutations in the PHEX, the causative gene in X-linked dominant hypophosphatemic rickets

Research output: Contribution to journalArticlepeer-review

Huda A. BinEssa, Minjing Zou, Anwar F. Al-Enezi, Basma Alomrani, Manar S. A. Al-Faham, Roua A. Al-Rijjal, Brian F. Meyer, Yufei Shi

Original languageEnglish
Pages (from-to)186-193
Published1 Aug 2019

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