Case of hypomagnesemia with secondary hypocalcemia with a novel TRPM6 mutation
Author:
Publisher
Medknow
Subject
Neurology (clinical),Neurology
Cited by 7 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. Intestinal hypomagnesemia in an Iranian patient with a novel TRPM6 variant: a case report and review of the literature;CEN Case Reports;2023-03-26
2. Familial Hypomagnesemia with Secondary Hypocalcemia Presenting as Refractory Seizures;Annals of Indian Academy of Neurology;2023
3. Case Report: Novel TRPM6 Mutations Cause Hereditary Hypomagnesemia With Secondary Hypocalcemia in a Chinese Family and a Literature Review;Frontiers in Pediatrics;2022-07-12
4. Hypomagnesemia with Secondary Hypoparathyroidism and Hypocalcemia due to Novel Variants in the Transient Receptor Potential Cation Channel Subfamily M Member 6 (TRPM6) Gene;Journal of Pediatric Genetics;2021-08-31
5. Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation;Journal of Clinical Research in Pediatric Endocrinology;2021-02-26
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