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Updated: Mar 31, 2026

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Disruption of Src Is Associated with Phenotypes Related to Williams-Beuren Syndrome and Altered Cellular Localization

Laleh Sinai1, Evgueni A Ivakine2, Emily Lam3

  • 1Institute of Medical Science, University of Toronto , Toronto, Ontario, M5S 1A8, Canada ; Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital , Toronto Ontario, M5S 3E1, Canada.

Eneuro
|October 15, 2015
PubMed

Keywords:
Src tyrosine kinaseWilliams-Beuren syndromecalcium channelgeneral transcription factor 2 Imouse behavior

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