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Publikováno v:
Rheumatology. 59
Background Hypophosphatasia (HPP) is a condition arising due to mutations in the gene encoding the tissue-non-specific alkaline phosphatase (TNSALP) isoenzyme (ALPL), leading to deficient activity of TNSALP. It can be inherited as an autosomal domina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e18f08b4263573760a3338d0b1c69396
https://doi.org/10.1093/rheumatology/keaa110
https://doi.org/10.1093/rheumatology/keaa110
