Results
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A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia. [electronic resource] by
- Hasan, Sonia
- Bove, Cecilia
- Silvestri, Gabriella
- Mantuano, Elide
- Modoni, Anna
- Veneziano, Liana
- Macchioni, Lara
- Hunter, Therese
- Hunter, Gary
- Pessia, Mauro
- D'Adamo, Maria Cristina
Producer: 20190110
In:
Scientific reports vol. 7
Availability: No items available.
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150.
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151.
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152.
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Optogenetic and potassium channel gene therapy in a rodent model of focal neocortical epilepsy. [electronic resource] by
- Wykes, Robert C
- Heeroma, Joost H
- Mantoan, Laura
- Zheng, Kaiyu
- MacDonald, Douglas C
- Deisseroth, Karl
- Hashemi, Kevan S
- Walker, Matthew C
- Schorge, Stephanie
- Kullmann, Dimitri M
Producer: 20130619
In:
Science translational medicine vol. 4
Availability: No items available.
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153.
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154.
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155.
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A de novo KCNA1 Mutation in a Patient with Tetany and Hypomagnesemia. [electronic resource] by
- van der Wijst, Jenny
- Konrad, Martin
- Verkaart, Sjoerd A J
- Tkaczyk, Marcin
- Latta, Femke
- Altmüller, Janine
- Thiele, Holger
- Beck, Bodo
- Schlingmann, Karl Peter
- de Baaij, Jeroen H F
Producer: 20190927
In:
Nephron vol. 139
Availability: No items available.
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158.
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Episodic ataxia type 1: clinical characterization, quality of life and genotype-phenotype correlation. [electronic resource] by
- Graves, Tracey D
- Cha, Yoon-Hee
- Hahn, Angelika F
- Barohn, Richard
- Salajegheh, Mohammed K
- Griggs, Robert C
- Bundy, Brian N
- Jen, Joanna C
- Baloh, Robert W
- Hanna, Michael G
Producer: 20140521
In:
Brain : a journal of neurology vol. 137
Availability: No items available.
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