A Propitous Genetic Impact on Neurodevelopmental Disorders - A Flagstone for Personalized Medicine

Authors

  • Sujitha P.J1 , V. Gomathi2

DOI:

https://doi.org/10.37506/ijphrd.v11i6.9924

Keywords:

genetics, whole – exome sequencing, whole genome sequencing, genomics, neurodevelopmental conditions, NDD

Abstract

There has been a precipitous advancement of unequivocal technological and methodological upgradings

in genetics and genomics, thereby allowing to identify atypical mutations that are involved in complex

neurodevelopmental conditions. Neoteric advancements in genomics such as whole – exome or whole

genome sequencing have endorsed scientist to identify extensive mutations underlying NDDS. In this

review we are recapitating the new-fangled developments in genomic analysis and deciphering it into

clinical practice.

Author Biography

  • Sujitha P.J1 , V. Gomathi2

    1PhD Research Scholar, Department of Pharmacology, Vinayaka Mission College of Pharmacy, Salem, Tamil

    Nadu, India. 2 Associate Professor, Department of Pharmacology, Vinayaka Mission College of Pharmacy, Salem,

    Tamil Nadu, India

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Published

2020-06-25

Issue

Vol. 11 No. 6 (2020): Indian Journal of Public Health Research & Development

Section

Articles

How to Cite

A Propitous Genetic Impact on Neurodevelopmental Disorders - A Flagstone for Personalized Medicine. (2020). Indian Journal of Public Health Research & Development, 11(6), 997-1003. https://doi.org/10.37506/ijphrd.v11i6.9924