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Tissue non-specific alkaline phosphatase activity and mineralization capacity of bi-allelic mutations from severe perinatal and asymptomatic hypophosphatasia phenotypes: Results from an in vitro mutagenesis model

Severe PerinatalDevelopmental BiologyGenetic DisorderGeneticsInherited Metabolic DiseaseProtein PhosphorylationMolecular GeneticsVitro Mutagenesis ModelMetabolismMedicineCell BiologyMineralization CapacityEmbryologyMutagenesis