Novel mutations in TRPM6 gene associated with primary hypomagnesemia with secondary hypocalcemia. Case report-Reference-Cited by-同舟云学术

Novel mutations in TRPM6 gene associated with primary hypomagnesemia with secondary hypocalcemia. Case report

Published:2021-11-23 Issue:4 Volume:165 Page:454-457
ISSN:1213-8118
Container-title:Biomedical Papers
language:
Short-container-title:BIOMED PAP

Author:

Papez Jan,Starha Jiri,Slaba Katerina,Hubacek Jaroslav A,Pecl Jakub,Aulicka Stefania,Urik Milan,Ceylaner Serdar,Vesela Petra,Slaby Ondrej,Jabandziev Petr

Publisher

Palacky University Olomouc

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://biomed.papers.upol.cz/doi/10.5507/bp.2021.027.pdf

Reference18 articles.

1. Lower serum magnesium concentration is associated with diabetes, insulin resistance, and obesity in South Asian and white Canadian women but not men

2. Magnesium in Prevention and Therapy

3. Assessment of magnesium status for diagnosis and therapy;Elin RJ;Magnes Res,2010

4. Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family

5. Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia

Cited by 3 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. Hereditary hypomagnesemia with secondary hypocalcemia caused by a novel mutation in TRPM6 gene;Journal of Pediatric Endocrinology and Metabolism;2023-12-13

2. 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

3. Case Report: A Novel Non-Canonical Splice Site Variant (c.1638+7T>C) in TRPM6 Cause Primary Homagnesemia With Secondary Hocalcemia;Frontiers in Pediatrics;2022-05-25