Novel mutation in potassium channel related gene KCTD7 and progressive myoclonic epilepsy.

Krabichler, Birgit

Novel mutation in potassium channel related gene KCTD7 and progressive myoclonic epilepsy. [electronic resource] - Annals of human genetics Jul 2012 - 326-31 p. digital

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

1469-1809

10.1111/j.1469-1809.2012.00710.x doi


Child
Chromosomes, Human, Pair 7
Genetic Linkage
Humans
Male
Mutation, Missense
Myoclonic Epilepsies, Progressive--genetics
Potassium Channels--genetics