Open AccessCNNM2 heterozygous variant presenting as hypomagnesemia and west syndrome: Expanding the spectrum of CNNM2 gene-related epileptic disorders
Author(s) -
Prateek Kumar Panda,
Radhapyari Lourembam,
Indar Kumar Sharawat
Publication year - 2021
Publication title -
annals of indian academy of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.427
H-Index - 31
eISSN - 1998-3549
pISSN - 0972-2327
DOI - 10.4103/aian.aian_1130_20
Subject(s) - hypomagnesemia , medicine , epilepsy , west syndrome , gene , genetics , pediatrics , psychiatry , biology , materials science , magnesium , metallurgy