Analysis of Localization of Mutated Tissue-Nonspecific Alkaline Phosphatase Proteins Associated with Neonatal Hypophosphatasia Using Green Fluorescent Protein Chimeras
Author:
Publisher
The Endocrine Society
Subject
Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Cited by 44 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. The Effect of Asfotase Alfa on Plasma and Urine Pyrophosphate Levels and Pseudofractures in a Patient With Adult‐Onset Hypophosphatasia;JBMR Plus;2023-11-20
2. A unique case of childhood hypophosphatasia caused by a novel heterozygous 51-bp in-frame deletion in the ALPL gene;CLIN PEDIATR ENDOCRI;2023
3. A unique case of childhood hypophosphatasia caused by a novel heterozygous 51-bp in-frame deletion in the <i>ALPL</i> gene;Clinical Pediatric Endocrinology;2023
4. Novel mutation in the ALPL gene with a dominant negative effect in a Japanese family;Journal of Bone and Mineral Metabolism;2021-04-05
5. Hypophosphatasia in Japan: ALPL Mutation Analysis in 98 Unrelated Patients;Calcified Tissue International;2019-11-09
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