Sawssan Ben Romdhan
2PUBLICATIONS
0CO-AUTHORS

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Publications (2)
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|Sep 07, 2018
A Novel SYNJ1 Mutation in a Tunisian Family with Juvenile Parkinson's Disease Associated with Epilepsy.Sawssan Ben Romdhan, Salma Sakka, Nouha Farhat
|Jul 11, 2018
LRRK2 G2019S Parkinson's disease with more benign phenotype than idiopathic.Sawssan Ben Romdhan, Nouha Farhat, Amina Nasri
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