Spectrum and frequencies of non <scp> <i>GJB2</i> </scp> gene mutations in Czech patients with early non‐syndromic hearing loss detected by gene panel NGS and whole‐exome sequencingDana Šafka Brožková, Pavel Seeman, Vlasta Čejnová et al.|Clinical Genetics|2020Cited by 35
The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes—A Comprehensive Study of the GJB2/DFNB1 RegionDana Šafka Brožková, Pavel Seeman, Anna Uhrová Mészárosová et al.|Genes|2021Cited by 21