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Drosophila Cav2 channels harboring human migraine mutations cause synapse hyperexcitability that can be suppressed by inhibition of a Ca2+ store release pathway
Douglas J. Brusich, Ashlyn M. Spring, Thomas D. James, Timothy H. Helms, View ORCID ProfileC. Andrew Frank
doi: https://doi.org/10.1101/141366
Douglas J. Brusich
1Department of Anatomy and Cell Biology, University of Iowa Carver College of Medicine, Iowa City, IA 52242
Ashlyn M. Spring
1Department of Anatomy and Cell Biology, University of Iowa Carver College of Medicine, Iowa City, IA 52242
2Interdisciplinary Graduate Program in Genetics, University of Iowa, Iowa City, IA 52242
Thomas D. James
1Department of Anatomy and Cell Biology, University of Iowa Carver College of Medicine, Iowa City, IA 52242
3Interdisciplinary Graduate Program in Neuroscience, University of Iowa, Iowa City, IA 52242
Timothy H. Helms
1Department of Anatomy and Cell Biology, University of Iowa Carver College of Medicine, Iowa City, IA 52242
C. Andrew Frank
1Department of Anatomy and Cell Biology, University of Iowa Carver College of Medicine, Iowa City, IA 52242
2Interdisciplinary Graduate Program in Genetics, University of Iowa, Iowa City, IA 52242
3Interdisciplinary Graduate Program in Neuroscience, University of Iowa, Iowa City, IA 52242
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Posted May 23, 2017.
Drosophila Cav2 channels harboring human migraine mutations cause synapse hyperexcitability that can be suppressed by inhibition of a Ca2+ store release pathway
Douglas J. Brusich, Ashlyn M. Spring, Thomas D. James, Timothy H. Helms, C. Andrew Frank
bioRxiv 141366; doi: https://doi.org/10.1101/141366
Drosophila Cav2 channels harboring human migraine mutations cause synapse hyperexcitability that can be suppressed by inhibition of a Ca2+ store release pathway
Douglas J. Brusich, Ashlyn M. Spring, Thomas D. James, Timothy H. Helms, C. Andrew Frank
bioRxiv 141366; doi: https://doi.org/10.1101/141366
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