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Updated: May 14, 2026

06:41
In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
Defining and refining the phenotype of PRRT2 mutations
1University of Rochester-Neurology, Rochester, NY, USA.
Developmental Medicine and Child Neurology
|February 1, 2013
Summary
No abstract available in PubMed .
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