No abstract available
MeSH terms
-
Calcium Channels, T-Type / genetics*
-
Channelopathies / genetics
-
Epilepsy / genetics*
-
Genetic Testing
-
Genetic Variation*
-
Humans
-
Mutation, Missense
-
Neurology / trends
Substances
-
CACNA1H protein, human
-
Calcium Channels, T-Type