Rare-variant association analysis reveals known and new age-related hearing loss genes

Cornejo-Sanchez, D. M., Li, G., Fabiha, T., Wang, R., Acharya, A., Everard, J. L., Kadlubowska, M. K., Huang, Y., Schrauwen, I., Wang, G. T., DeWan, A. T., & Leal, S. M. (2023). Rare-variant association analysis reveals known and new age-related hearing loss genes. European Journal of Human Genetics, 31(6), 638–647. https://doi.org/10.1038/s41431-023-01302-2
Authors:
Diana M Cornejo-Sanchez
Guangyou Li
Tabassum Fabiha
Ran Wang
Anushree Acharya
Jenna L Everard
Magda K Kadlubowska
Yin Huang
Isabelle Schrauwen
Gao T Wang
Andrew T DeWan
Suzanne M Leal
Affiliated Authors:
Diana M Cornejo-Sanchez
Guangyou Li
Tabassum Fabiha
Ran Wang
Anushree Acharya
Jenna L Everard
Magda K Kadlubowska
Yin Huang
Isabelle Schrauwen
Gao T Wang
Suzanne M Leal
Subjects:
Presbycusis (MeSH)
Publication Type:
Article
Unique ID:
10.1038/s41431-023-01302-2
PMID:
Publication Date:
Data Source:
PubMed

Record Created: