טוען...
Adult hypophosphatasia with a novel ALPL mutation: Report of an Indian kindred
Hypophosphatasia is an inborn error in metabolism characterized by low serum alkaline phosphatase (ALP) activity resulting from deactivating mutations in TNSALP (also known as ALPL), the gene that encodes the ‘tissue-specific’ isoenzyme of ALP. The disease exhibits significant clinical heterogeneity...
שמור ב:
| הוצא לאור ב: | Bone Rep |
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| Main Authors: | , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Elsevier
2020
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6997823/ https://ncbi.nlm.nih.gov/pubmed/32025537 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bonr.2020.100247 |
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