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
Dana Šafka Brožková(Charles University), Pavel Seeman, Anna Uhrová Mészárosová(Charles University), Jana Laštůvková(Krajská Zdravotní), Andrej Ficek(Comenius University Bratislava), Martina Škopková(Institute of Experimental Endocrinology of the Slovak Academy of Sciences), Andrea Šoltýsová(Slovak Academy of Sciences), Ján Jenčík(Charles University), Daniela Gašperíková(Institute of Chemistry of the Slovak Academy of Sciences), Zuzana Slobodová(Slovak Academy of Sciences), Lukáš Varga(Slovak Academy of Sciences)
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