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, Simona Poisson Marková et al.|Clinical Genetics|2020Cited by 35
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, Zuzana Slobodová et al.|Orphanet Journal of Rare Diseases|2020Cited by 15
Two types of recessive hereditary spastic paraplegia in Roma patients in compound heterozygous state; no ethnically prevalent variant foundAnna Uhrová Mészárosová, Dana Šafka Brožková, Pavel Seeman et al.|Neuroscience Letters|2020Cited by 12
Author response for "Spectrum and frequencies of non <scp> <i>GJB2</i> </scp> gene mutations in Czech patients with early non‐syndromic hearing loss detected by <scp>NGS</scp> gene panel and <scp>WES</scp>"Dana Šafka Brožková, Pavel Seeman, Simona Poisson Marková et al.|Unknown|2020Cited by 0
Author response for "Spectrum and frequencies of non <scp> <i>GJB2</i> </scp> gene mutations in Czech patients with early non‐syndromic hearing loss detected by <scp>NGS</scp> gene panel and <scp>WES</scp>"Dana Šafka Brožková, Pavel Seeman, Simona Poisson Marková et al.|Unknown|2020Cited by 0