Yu-Mian Gan
2PUBLICATIONS
9CO-AUTHORS

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Publications (2)
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|Jun 02, 2022
Function of PHEX mutations p.Glu145* and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription.Yu-Mian Gan, Yan-Ping Zhang, Dan-Dan Ruan
|Nov 16, 2021
Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family.Wen Wei, Xiu-Fen Zheng, Dan-Dan Ruan
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