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Updated: Dec 24, 2025

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Novel variants and uncommon cases among southern Chinese children with X-linked hypophosphatemia

Y Lin1, J Xu1, X Li1

  • 1Department of Genetics and Endocrinology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, 9 Jinsui Rd., Guangzhou, 510623, China.

Journal of Endocrinological Investigation
|April 8, 2020
PubMed
Abstract

Keywords:
Clinical featuresMutational spectrumPHEX geneSouthern ChinaX-linked hypophosphatemia

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