S-EPMC8680880 - CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndrome: Expanding the Spectrum of CNNM2 Gene-Related Epileptic Disorders. - OmicsDI

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

ABSTRACT:

SUBMITTER: Panda PK

PROVIDER: S-EPMC8680880 | biostudies-literature | 2021 Sep-Oct

REPOSITORIES: biostudies-literature