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Identification of a Novel Missense Mutation of the PHEX Gene in a Large Chinese Family with X-Linked Hypophosphataemia https://t.co/XJIsdBsFgL
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New Research: Identification of a Novel Missense Mutation of the PHEX Gene in a Large Chinese Family with X-Linked Hypophosphataemia: X-linked hypophosphataemia (XLH) is an X-linked dominant rare disease that refers to the most common… https://t.co/QtnpMtX