KCNJ10 mutations display differential sensitivity to heteromerisation with KCNJ16.

Parrock, Sophie

KCNJ10 mutations display differential sensitivity to heteromerisation with KCNJ16. [electronic resource] - Nephron. Physiology 2013 - 7-14 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1660-2137

10.1159/000356353 doi


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