TY  - GEN
AU  - Krabichler,Birgit
AU  - Rostasy,Kevin
AU  - Baumann,Matthias
AU  - Karall,Daniela
AU  - Scholl-Bürgi,Sabine
AU  - Schwarzer,Christoph
AU  - Gautsch,Kurt
AU  - Spreiz,Ana
AU  - Kotzot,Dieter
AU  - Zschocke,Johannes
AU  - Fauth,Christine
AU  - Haberlandt,Edda
TI  - Novel mutation in potassium channel related gene KCTD7 and progressive myoclonic epilepsy
SN  - 1469-1809
PY  - 2012///0822
KW  - Child
KW  - Chromosomes, Human, Pair 7
KW  - Genetic Linkage
KW  - Humans
KW  - Male
KW  - Mutation, Missense
KW  - Myoclonic Epilepsies, Progressive
KW  - genetics
KW  - Potassium Channels
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/j.1469-1809.2012.00710.x
ER  -