https://www.selleckchem.com/pr....oducts/nms-p937-nms1
Hypophosphatasia (HPP) is a rare hereditary disorder characterized by defective bone and tooth mineralization caused by mutations in the alkaline phosphatase ( ) gene encoding tissue-nonspecific alkaline phosphatase (TNSALP). Here we performed clinical and molecular studies on 5 HPP children to investigate the pathogenic mechanisms of the gene variants. Clinical and genetic analyses were performed on 5 HPP children, and the loci where variants were identified. Plasmids containing the relevant loci were constructed. The molec
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