![PDF) 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 PDF) 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](https://i1.rgstatic.net/publication/343891881_Variant_c2158-2AG_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/links/5f523c5792851c250b8f698f/largepreview.png)
PDF) 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
Český rozhlas Karlovy Vary - My z rozhlasu! :) (zleva: Jitka Brožková, Andrea Vajnar, Dana Jelínková, Jana Strejčková, Jaroslav Ladýř, Marek Štětina, Radek Bílský, Libuše Ernestová, Radim Jehlík, David Forst, Lukáš Staněk,
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Iveta BROŽKOVÁ | University of Pardubice, Pardubice | Department of Biological and Biochemical Sciences | Research profile
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