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View article: 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 variant
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 variant Open
View article: 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>"
Author response for "Spectrum and frequencies of non <span> <i>GJB2</i> </span> gene mutations in Czech patients with early non‐syndromic hearing loss detected by <span>NGS</span> gene panel and <span>WES</span>" Open
View article: 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>"
Author response for "Spectrum and frequencies of non <span> <i>GJB2</i> </span> gene mutations in Czech patients with early non‐syndromic hearing loss detected by <span>NGS</span> gene panel and <span>WES</span>" Open