Hypophosphatasia: Vitamin B6 status of affected children and adults.
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DOI: 10.1016/j.bone.2021.116204
Abstract: Hypophosphatasia (HPP) is the heritable dento-osseous disease caused by loss-of-function mutation(s) of the gene ALPL that encodes the tissue-nonspecific isoenzyme of alkaline phosphatase (TNSALP). TNSALP is a cell-surface homodimeric phosphomonoester phosphohydrolase expressed in healthy people… read more here.
Keywords: affected children; plp; children adults; hpp ... See more keywords