EFHC1 mutation in Indian juvenile myoclonic epilepsy patient

OBJECTIVE: Juvenile myoclonic epilepsy (JME) is the most common form of idiopathic generalized epilepsies (IGEs) and is genetically heterogeneous. Mutations in EFHC1 cause JME. Because about 2 million people in India are affected by JME alone, we investigated the prevalence of mutations in the EFHC1...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Epilepsia Open
Autors principals: Thounaojam, Romita, Langbang, Leader, Itisham, Kavish, Sobhani, Roohollah, Srivastava, Shivani, Ramanujam, Bhargavi, Verma, Ramesh, Tripathi, Manjari, Aguan, Kripamoy
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2017
Matèries:
Full‐length Original Research
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5939392/
https://ncbi.nlm.nih.gov/pubmed/29750216
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/epi4.12037
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars