Publications
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Auteur Title [ Type
Filtres: Auteur is Sadaghiani, Shokufeh [Enlever les filtres]
Genome-wide variant by serum urate interaction in Parkinson's disease.. Ann Neurol. 78(5):731-41.
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2015. Channelopathy-related SCN10A gene variants predict cerebellar dysfunction in multiple sclerosis.. Neurology. 86(5):410-7.
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2016.