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
Select a paper to view details