Associated Papers
Two novel variants in CNNM2 disrupts magnesium efflux leading to neurodevelopmental disorders.
Li H et al.
Frontiers in Genetics, 2025
New insights into the structure and function of CNNM proteins.
Chen YS et al.
The Febs Journal, 2023
Rare hypomagnesemia, seizures, and mental retardation in a 4-month-old patient caused by novel CNNM2 mutation Tyr189Cys: Genetic analysis and review.
Xu X et al.
Molecular Genetics & Genomic Medicine, 2022
35170241 (PubMed )
Supplement: MGG3-10-e1898-s001.xlsx › Sheet1
Novel CNNM2 Mutation Responsible for Autosomal-Dominant Hypomagnesemia With Seizure.
Tseng MH et al.
Frontiers in Genetics, 2022
Crystal structure of an archaeal CorB magnesium transporter.
Chen YS et al.
Nature Communications, 2021
Case Report: CNNM2 Mutations Cause Damaged Brain Development and Intractable Epilepsy in a Patient Without Hypomagnesemia.
Li X et al.
Frontiers in Genetics, 2021
CNNM2-Related Disorders: Phenotype and Its Severity Were Associated With the Mode of Inheritance.
Zhang H et al.
Frontiers in Pediatrics, 2021
Novel variant in the CNNM2 gene associated with dominant hypomagnesemia.
García-Castaño A et al.
Plos One, 2020
CNNM2 homozygous mutations cause severe refractory hypomagnesemia, epileptic encephalopathy and brain malformations.
Accogli A et al.
European Journal of Medical Genetics, 2019
CNNM2 mutations cause impaired brain development and seizures in patients with hypomagnesemia.
Arjona FJ et al.
Plos Genetics, 2014
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