Title : Mutational and biochemical findings in adults with persistent hypophosphatasemia.

Pub. Date : 2017 Aug

PMID : 28401263






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 In HPP, ALPL mutations result in persistent hypophosphatasemia and ALP substrate accumulation in plasma (pyridoxal-5-phosphate (PLP)) and urine (phosphoethanolamine (PEA)). Pyridoxal Phosphate alkaline phosphatase, placental Homo sapiens
2 In HPP, ALPL mutations result in persistent hypophosphatasemia and ALP substrate accumulation in plasma (pyridoxal-5-phosphate (PLP)) and urine (phosphoethanolamine (PEA)). Pyridoxal Phosphate alkaline phosphatase, placental Homo sapiens