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![Spectrum of <i>MECP2</i> mutations in Indian females with Rett Syndrome - a large cohort study](https://image.oaes.cc/1ed76e9f-0266-4e29-9070-bdafb2f2fb4f/3461.fig.1.jpg)
Figure 1. Sequencing chromatograms of novel MECP2 variants identified in RTT patients in present study: A: frameshift variant p.G92X; B: missense variant p.L138S; C: frameshift variant p.R162fs; D: frameshift variant p. E290fs; E: frameshift variant p.V485fs; and F: frameshift variant p. S486fs