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. Author manuscript; available in PMC: 2013 Sep 4.
Published in final edited form as: Neurobiol Dis. 2012 Oct 13;50:135–141. doi: 10.1016/j.nbd.2012.10.008

Fig. 1.

Fig. 1

GABRG2(S443delC) mutation was identified in a GEFS+ family. (A) Pedigree of the family with GEFS+. The arrow points to the proband. (B) EEG from patient III:4 showing a burst of generalized epileptiform abnormalities.