Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene.

Added 2902 days ago (14.06.2012)
Authors: Kousi M, Anttila V, Schulz A, Calafato S, Jakkula E, Riesch E, Myllykangas L, Kalimo H, Topçu M, Gökben S, Alehan F, Lemke JR, Alber M, Palotie A, Kopra O, Lehesjoki AE
PubMed id: 22693283
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