Associated Papers
Molecular Diagnoses of X-Linked and Other Genetic Hypophosphatemias: Results From a Sponsored Genetic Testing Program.
Rush ET et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research, 2022
34633109 (PubMed )
Supplement: JBMR-37-202-s001.xlsx › Supplemental_Table_2
A rare mutation in hypophosphatasia: a case report of adult form and review of the literature.
Galeano-Valle F et al.
Archives of Endocrinology and Metabolism, 2019
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