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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… Click to show full abstract
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 gene in the Indian population with JME. We studied 63 patients with JME and 80 healthy controls.
Keywords:
jme;
myoclonic epilepsy;
efhc1 mutation;
juvenile myoclonic
Journal Title: Epilepsia Open
Year Published: 2017
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Journal Title: Epilepsia Open
Year Published: 2017
Link to full text (if available)
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recommendations!