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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy

Fadi F Hamdan1, Amélie Piton, Julie Gauthier

  • 1Centre of Excellence in Neuromics of Université de Montréal and Synapse to Disease Group, Centre Hospitalier Universitaire Sainte-Justine Research Center, Université de Montréal, Montreal, Quebec, Canada.

Annals of Neurology
|June 27, 2009
PubMed

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