The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes—A Comprehensive Study of the GJB2/DFNB1 RegionDana Šafka Brožková, Pavel Seeman, David Staněk et al.|Genes|2021Cited by 21
Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variantDana Šafka Brožková, Pavel Seeman, Lukáš Varga et al.|Orphanet Journal of Rare Diseases|2020Cited by 15