KCNJ10 mutations display differential sensitivity to heteromerisation with KCNJ16. [electronic resource]
Producer: 20140625Description: 7-14 p. digitalISSN:- 1660-2137
- Alanine -- genetics
- Animals
- Female
- Genotype
- Hearing Loss, Sensorineural -- genetics
- Humans
- Intellectual Disability -- genetics
- Oocytes -- metabolism
- Patch-Clamp Techniques
- Point Mutation
- Potassium Channels, Inwardly Rectifying -- chemistry
- Protein Multimerization
- Seizures -- genetics
- Sequence Analysis, DNA
- Valine -- genetics
- Xenopus
- Kcnj10 Channel
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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