Utility of Whole Genome Sequencing for Population Screening of Deafness-Related Genetic Variants and Cytomegalovirus Infection in Newborns

Background: Hearing loss affects approximately two out of every 1,000 newborns. Genetic factors and congenital cytomegalovirus (CMV) infections account for around 90% of the etiology. The purpose of this study was to develop and test a whole genome sequencing (WGS) approach to detect deafness-relate...

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Detalles Bibliográficos
Autores principales: Xiang, Jiale, Zhang, Hongfu, Sun, Xiangzhong, Zhang, Junqing, Xu, Zhenpeng, Sun, Jun, Peng, Zhiyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099144/
https://www.ncbi.nlm.nih.gov/pubmed/35571039
http://dx.doi.org/10.3389/fgene.2022.883617

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099144/
https://www.ncbi.nlm.nih.gov/pubmed/35571039
http://dx.doi.org/10.3389/fgene.2022.883617

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