A Novel SYNJ1 Mutation in a Tunisian Family with Juvenile Parkinson’s Disease Associated with Epilepsy

Overview of attention for article published in Journal of Molecular Neuroscience, September 2018

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A new genetic variation in the SYNJ1 gene has been discovered in a Tunisian family, which is associated with juvenile onset #Parkinsons & #epilepsy https://t.co/nuTJQTMHdO https://t.co/l2gg76Q6Ke

PubMed: A Novel SYNJ1 Mutation in a Tunisian Family with Juvenile Parkinson's Disease Associated with Epilepsy. https://t.co/ros2HxysNH

A Novel SYNJ1 Mutation in a Tunisian Family with Juvenile Parkinson's Disease Associated with Epilepsy. https://t.co/yIaWBWBICY