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An X-linked channelopathy with cardiomegaly due to a CLIC2 mutation enhancing ryanodine receptor channel activity. [electronic resource] by
- Takano, Kyoko
- Liu, Dan
- Tarpey, Patrick
- Gallant, Esther
- Lam, Alex
- Witham, Shawn
- Alexov, Emil
- Chaubey, Alka
- Stevenson, Roger E
- Schwartz, Charles E
- Board, Philip G
- Dulhunty, Angela F
Producer: 20130621
In:
Human molecular genetics vol. 21
Availability: No items available.
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487.
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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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