Pathophysiology of hypophosphatasia and the potential role of asfotase alfa
Pathophysiology of hypophosphatasia and the potential role of asfotase alfa
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New Zealand: Dove Medical Press Limited
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English
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New Zealand: Dove Medical Press Limited
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Hypophosphatasia (HPP) is an inherited systemic bone disease that is characterized by bone hypomineralization. HPP is classified into six forms according to the age of onset and severity as perinatal (lethal), perinatal benign, infantile, childhood, adult, and odontohypophosphatasia. The causative gene of the disease is the ALPL gene that encodes t...
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Pathophysiology of hypophosphatasia and the potential role of asfotase alfa
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TN_cdi_doaj_primary_oai_doaj_org_article_9456a692ab4b4e0e8818ab6e0f05fa20
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_9456a692ab4b4e0e8818ab6e0f05fa20
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ISSN
1176-6336,1178-203X
E-ISSN
1178-203X
DOI
10.2147/TCRM.S87956
