Zobrazeno 1 - 1
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pro vyhledávání: '"Rafi Brener"'
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
An inactivating PHEX gene mutation with the resultant accumulation of several mineralization-inhibiting proteins (e.g., FGF23) causes skeletal and dental morbidity in X-linked hypophosphatemia (XLH). This prospective case-control study explored the e
Externí odkaz:
https://doaj.org/article/3a718105cf11478fa9c620810512fe72