Mutational Analysis of Myoclonin1 Gene in Pakistani Juvenile Myoclonic Epilepsy Patients

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 (EFHC1) encodes for a nonion channel protein and mutations in this gene have been extensively...

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Detalles Bibliográficos
Autores principales: Saleem, Tayyaba, Mustafa, Arooj, Sheikh, Nadeem, Mukhtar, Maryam, Irfan, Mavra, Suqaina, Saira Kainat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8081613/
https://www.ncbi.nlm.nih.gov/pubmed/33969125
http://dx.doi.org/10.1155/2021/7509825

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