Associated Papers
Two novel variants in CNNM2 disrupts magnesium efflux leading to neurodevelopmental disorders.
Li H et al.
Frontiers in Genetics, 2025
40612795 (PubMed )
Supplement: Supplementaryfile1.docx
New insights into the structure and function of CNNM proteins.
Chen YS et al.
The Febs Journal, 2023
CNNM2-Related Disorders: Phenotype and Its Severity Were Associated With the Mode of Inheritance.
Zhang H et al.
Frontiers in Pediatrics, 2021
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