← Evidence map

ArticleAnnals of Indian Academy of Neurology

CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndrome: Expanding the Spectrum of CNNM2 Gene-Related Epileptic Disorders.

Prateek K Panda et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

3 papers cite it

2024
2025
2026
cites it
Full record →Abstract, authors, funding and every citing paper · PMID 35002148