Publication | Open Access

Prevalence of c.1559delT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypophosphatasia in Japanese and effects of the mutation on heterozygous carriers

BiologyAllelic VariantMendelian DisorderCommon MutationHeterozygous CarriersGeneticsMedicineGenetic EpidemiologyGenetic DisorderPathologyGenetic VariationPublic HealthPopulation GeneticsGenetic Basis