A novel homozygous w99g mutation in cldn-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in turkish siblings-Reference-Cited by-同舟云学术

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A novel homozygous w99g mutation in cldn-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in turkish siblings

Published:2018 Issue:1 Volume:60 Page:76
ISSN:0041-4301
Container-title:The Turkish Journal of Pediatrics
language:
Short-container-title:TurkJPediatr

Author:

Alparslan Caner,Öncel Elif Perihan,Akbay Sinem,Alaygut Demet,Mutlubaş Fatma,Tatlı Mansur,Konrad Martin,Yavaşcan Önder,Kasap-Demir Belde

Publisher

The Turkish Journal of Pediatrics

Subject

Pediatrics, Perinatology and Child Health

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. Ocular manifestations of the genetic renal tubulopathies;Ophthalmic Genetics;2023-09-13

2. Evaluation of Phenotypes and CLDN16 Variants in 2 Different Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Families: Phenotypic Differences in Siblings and Phenotypic Similarity in Monozygotic Twins;Turkish Journal of Nephrology;2023-01-04

3. Possible prospects for using modern magnesium preparations for increasing stress resistance during COVID-19 pandemic;Research Results in Pharmacology;2020-12-29

4. Claudins in Renal Physiology and Pathology;Genes;2020-03-10

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