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Whole exome sequencing uncovered highly penetrant recessive mutations for a spectrum of rare genetic pediatric diseases in Bangladesh

Lookup NU author(s): Dr Marc Woodbury-Smith



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Publication metadata

Author(s): Akter H, Hossain M, Dity N, Rahaman A, Uddin KM, Nassir N, Begum G, Hameid R, Islam M, Tusti T, Basiruzzaman M, Sarkar S, Islam M, Jahan S, Lim E, Woodbury-Smith M, Stavropoulos D, O'Rielly D, Berdeiv B, Nabi AHM, Ahsan M, Scherer SW, Uddin M

Publication type: Article

Publication status: Published

Journal: npj Genomic Medicine

Year: 2021

Volume: 6

Online publication date: 16/02/2021

Acceptance date: 06/01/2021

Date deposited: 09/03/2021

ISSN (electronic): 2056-7944

Publisher: Nature Publishing Group


DOI: 10.1038/s41525-021-00173-0


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Funder referenceFunder name
Al Jalila Foundation
College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences
Genetics and Genomic Medicine Centre, NeuroGen Children's Healthcare grant