Fig. 4From: Chinese cases of early infantile epileptic encephalopathy: a novel mutation in the PCDH19 gene was proved in a mosaic male- case reportSchematic diagram of the point mutations identified in the PCDH19 gene. SP: signal peptide; EC: extracellular cadherin domain; TM: transmembrane domain; CM1 and CM2; cytoplasmic domains 1 and 2Back to article page