Associated Papers
Severe perinatal hypophosphatasia case with a novel mutation.
Yazici H et al.
Archivos Argentinos De Pediatria, 2022
Incidence of Mutations in the ALPL, GGPS1, and CYP1A1 Genes in Patients With Atypical Femoral Fractures.
Peris P et al.
Jbmr Plus, 2019
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