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  Published Paper Details:

  Paper Title

MECP2 PROTEIN IN RETT SYNDROME AND AUTISM.

  Authors

  Shweta Das

  Keywords

RETT syndrome (RTT), Autism, MeCP2 gene

  Abstract


RETT syndrome is an x-linked dominant disorder and results in improper development of the nervous system. Previous studies show that the disease usually occurs due to the mutation in the MeCP2 gene and thus the MeCP2 protein that thus in the MeCP2 protein which functions as a transcription suppressor. autism is also a neurodevelopmental disorder where the affected individuals do not show proper brain growth and development. Even though the genetic analysis of autistic patients shows complex genetic mechanism however, the role of MeCP2 protein in autism is still not very clear. This paper explains both the diseases as well as the role of MeCP2 protein in both the diseases. The paper also summarizes the experiment performed on 69 autistic female patients to observe the role of MeCP2 proteins in them.

  IJCRT's Publication Details

  Unique Identification Number - IJCRT2102105

  Paper ID - 202948

  Page Number(s) - 837-842

  Pubished in - Volume 9 | Issue 2 | February 2021

  DOI (Digital Object Identifier) -    http://doi.one/10.1729/Journal.25732

  Publisher Name - IJCRT | www.ijcrt.org | ISSN : 2320-2882

  E-ISSN Number - 2320-2882

  Cite this article

  Shweta Das,   "MECP2 PROTEIN IN RETT SYNDROME AND AUTISM.", International Journal of Creative Research Thoughts (IJCRT), ISSN:2320-2882, Volume.9, Issue 2, pp.837-842, February 2021, Available at :http://www.ijcrt.org/papers/IJCRT2102105.pdf

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ISSN: 2320-2882
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Journal Starting Year (ESTD) : 2013
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ISSN and 7.97 Impact Factor Details


ISSN
ISSN
ISSN: 2320-2882
Impact Factor: 7.97 and ISSN APPROVED
Journal Starting Year (ESTD) : 2013
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