Electrophysiological characterization of a Ca
CACNA1H
Calcium channels
Cav3.2
Channelopathy
Epilepsy
Hearing
Ion channels
Mutation
T-type channels
Journal
Molecular brain
ISSN: 1756-6606
Titre abrégé: Mol Brain
Pays: England
ID NLM: 101468876
Informations de publication
Date de publication:
21 09 2023
21 09 2023
Historique:
received:
14
08
2023
accepted:
14
09
2023
medline:
25
9
2023
pubmed:
22
9
2023
entrez:
22
9
2023
Statut:
epublish
Résumé
T-type calcium channelopathies encompass a group of human disorders either caused or exacerbated by mutations in the genes encoding different T-type calcium channels. Recently, a new heterozygous missense mutation in the CACNA1H gene that encodes the Ca
Identifiants
pubmed: 37735453
doi: 10.1186/s13041-023-01058-2
pii: 10.1186/s13041-023-01058-2
pmc: PMC10515227
doi:
Substances chimiques
Calcium Channels
0
Types de publication
Case Reports
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
68Informations de copyright
© 2023. Min Zhuo, Bong-Kiun Kaang and BioMed central Ltd.
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