Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects

Gholipoorfeshkecheh, R. and Agarwala, S. and G, K. and Krishnappa, S. and Savitha, M. R. and Ramachandra, N. B. (2020) Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects. Egyptian Journal of Medical Human Genetics, 21 (1).

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Official URL: https://www-scopus-com-vtuconsortia.new.knimbus.co...
Item Type: Article
Additional Information: cited By 0
Subjects: B Life Science > Genetics and Genomics
Divisions: Department of > Genetics and Genomics
Depositing User: Mr Umendra uom
Date Deposited: 05 Oct 2021 06:28
Last Modified: 05 Oct 2021 06:28
URI: http://eprints.uni-mysore.ac.in/id/eprint/15813

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