Mutational Analysis of Myoclonin1 Gene in Pakistani Juvenile Myoclonic Epilepsy Patients.
Journal
BioMed research international
ISSN: 2314-6141
Titre abrégé: Biomed Res Int
Pays: United States
ID NLM: 101600173
Informations de publication
Date de publication:
2021
2021
Historique:
received:
22
07
2020
revised:
03
02
2021
accepted:
10
04
2021
entrez:
10
5
2021
pubmed:
11
5
2021
medline:
27
5
2021
Statut:
epublish
Résumé
Juvenile myoclonic epilepsy (JME) is the most prevalent and genetically heterogeneous form of epilepsy and accounts for 10-30% of all the cases worldwide. Ef-hand domain- (c-terminal-) containing protein 1 (
Identifiants
pubmed: 33969125
doi: 10.1155/2021/7509825
pmc: PMC8081613
doi:
Substances chimiques
Calcium-Binding Proteins
0
EFHC1 protein, human
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
7509825Informations de copyright
Copyright © 2021 Tayyaba Saleem et al.
Déclaration de conflit d'intérêts
The authors declare that there is no conflict of interest regarding the publication of this paper.
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