Fig. 2From: A rare case of a male child with post-zygotic de novo mosaic variant c.538C > T in MECP2 gene: a case report of Rett syndromeSchematic representation of MECP2 protein along with the corresponding domains and variants observed in mosaic males. Variant highlighted in red corresponds to the present case. Solid and broken arrows correspond to the variants associated with and without seizure phenotype, respectivelyBack to article page