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Abstract

nRett Syndrome (RTT) is a genetic brain disorder which typically becomes apparent after 6 to 18 months of age in females synonymized as “Cerebroatrophic hyperammonemia”. It is due to genetic mutation of the MECP2 gene present on the X-chromosome. Develops as a new mutation withn

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References

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Research & Reviews: A Journal of Neuroscience

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[if 344 not_equal=””]ISSN: 2277-6427[/if 344]

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