Tag: pet28a pdk2

A compound heterozygous mutation of the alkaline phosphatase ALPL gene causes hypophosphatasia in a Han Chinese familyA compound heterozygous mutation of the alkaline phosphatase ALPL gene causes hypophosphatasia in a Han Chinese family

| Steven Washington | 0 Comment

Hypophosphatasia (HPP) is a uncommon hereditary systemic illness that’s characterised by faulty bone and/or dental mineralization, and is brought on by mutations within the alkaline phosphatase gene (ALPL). The current