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• Published Ahead of print Open access Article 15 Mar 2023

  X - Chromosome Linked Rett Syndrome

  By Zeel Shah

  Abstract: Rett 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 with

  Published in Research and Reviews: A Journal of Neuroscience Read article →