Genetic basis of hereditary hypophosphataemic rickets and phenotype presentation in children and adults-Reference-Cited by-同舟云学术

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Genetic basis of hereditary hypophosphataemic rickets and phenotype presentation in children and adults

Published:2021-08-11 Issue:4 Volume:72 Page:366-394
ISSN:2299-8306
Container-title:Endokrynologia Polska
language:
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Author:

Tavana Nahid,Thilakavathy Karuppiah,Kennerson Marina L.,Ting Tzer Hwu

Publisher

VM Media SP. zo.o VM Group SK

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Cited by 4 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. Vitamin D in dentoalveolar and oral health;Feldman and Pike' s Vitamin D;2024

2. X-Linked Familial Hypophosphatemia: A Case Report of 27-Year Old Male and Review of Literature;Hormone and Metabolic Research;2023-10

3. Whole exome sequencing identifies two novel variants in PHEX and DMP1 in Malaysian children with hypophosphatemic rickets;Italian Journal of Pediatrics;2022-12-08

4. Shedding Light on the Complex Regulation of FGF23;Metabolites;2022-04-28

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