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Open Access
Peer-reviewed
Research Article
MARVELD2 (DFNB49) Mutations in the Hearing Impaired Central European Roma Population - Prevalence, Clinical Impact and the Common Origin
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Ivica Mašindová ,
Contributed equally to this work with: Ivica Mašindová, Andrea Šoltýsová, Lukáš Varga
Affiliation Laboratory of Diabetes and Metabolic Disorders & DIABGENE, Institute of Experimental Endocrinology, Slovak Academy of Sciences, Bratislava, Slovakia
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Andrea Šoltýsová ,
Contributed equally to this work with: Ivica Mašindová, Andrea Šoltýsová, Lukáš Varga
Affiliations Department of Molecular Biology, Faculty of Natural Sciences, Comenius University, Bratislava, Slovakia, Institute of Molecular Physiology and Genetics, Slovak Academy of Sciences, Bratislava, Slovakia
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Lukáš Varga ,
Contributed equally to this work with: Ivica Mašindová, Andrea Šoltýsová, Lukáš Varga
Affiliations Laboratory of Diabetes and Metabolic Disorders & DIABGENE, Institute of Experimental Endocrinology, Slovak Academy of Sciences, Bratislava, Slovakia, Department of Otorhinolaryngology—Head and Neck Surgery, Faculty of Medicine and University Hospital, Comenius University, Bratislava, Slovakia
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Petra Mátyás,
Affiliation Department of Medical Genetics, University of Pécs, Clinical Centre, Pécs, Hungary
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Andrej Ficek,
Affiliation Department of Molecular Biology, Faculty of Natural Sciences, Comenius University, Bratislava, Slovakia
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Miloslava Hučková,
Affiliations Laboratory of Diabetes and Metabolic Disorders & DIABGENE, Institute of Experimental Endocrinology, Slovak Academy of Sciences, Bratislava, Slovakia, Center for Molecular Medicine, Slovak Academy of Sciences, Bratislava, Slovakia
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Martina Sůrová,
Affiliation Laboratory of Diabetes and Metabolic Disorders & DIABGENE, Institute of Experimental Endocrinology, Slovak Academy of Sciences, Bratislava, Slovakia
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Dana Šafka-Brožková,
Affiliation DNA Laboratory, Department of Paediatric Neurology, Charles University 2nd Medical School and University Hospital Motol, Prague, Czech Republic
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Saima Anwar,
Affiliation Department of Otorhinolaryngology Head & Neck Surgery, School of Medicine, University of Maryland, Baltimore, Maryland, United States of America
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Judit Bene,
Affiliations Department of Medical Genetics, University of Pécs, Clinical Centre, Pécs, Hungary, Szentagothai Research Centre, University of Pécs, Pécs, Hungary
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Slavomír Straka,
Affiliation Department of Otorhinolaryngology—Head and Neck Surgery, Faculty Hospital of J. A. Reiman, Prešov, Slovakia
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Ingrid Janicsek,
Affiliation Department of Medical Genetics, University of Pécs, Clinical Centre, Pécs, Hungary
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Zubair M. Ahmed,
Affiliation Department of Otorhinolaryngology Head & Neck Surgery, School of Medicine, University of Maryland, Baltimore, Maryland, United States of America
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Pavel Seeman,
Affiliation DNA Laboratory, Department of Paediatric Neurology, Charles University 2nd Medical School and University Hospital Motol, Prague, Czech Republic
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Béla Melegh,
Affiliations Department of Medical Genetics, University of Pécs, Clinical Centre, Pécs, Hungary, Szentagothai Research Centre, University of Pécs, Pécs, Hungary
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Milan Profant,
Affiliation Department of Otorhinolaryngology—Head and Neck Surgery, Faculty of Medicine and University Hospital, Comenius University, Bratislava, Slovakia
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Iwar Klimeš,
Affiliation Laboratory of Diabetes and Metabolic Disorders & DIABGENE, Institute of Experimental Endocrinology, Slovak Academy of Sciences, Bratislava, Slovakia
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Saima Riazuddin,
Affiliation Department of Otorhinolaryngology Head & Neck Surgery, School of Medicine, University of Maryland, Baltimore, Maryland, United States of America
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Ľudevít Kádasi,
Affiliations Department of Molecular Biology, Faculty of Natural Sciences, Comenius University, Bratislava, Slovakia, Institute of Molecular Physiology and Genetics, Slovak Academy of Sciences, Bratislava, Slovakia
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Daniela Gašperíková
* E-mail: daniela.gasperikova@savba.sk
Affiliations Laboratory of Diabetes and Metabolic Disorders & DIABGENE, Institute of Experimental Endocrinology, Slovak Academy of Sciences, Bratislava, Slovakia, Center for Molecular Medicine, Slovak Academy of Sciences, Bratislava, Slovakia
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MARVELD2 (DFNB49) Mutations in the Hearing Impaired Central European Roma Population - Prevalence, Clinical Impact and the Common Origin
- Ivica Mašindová,
- Andrea Šoltýsová,
- Lukáš Varga,
- Petra Mátyás,
- Andrej Ficek,
- Miloslava Hučková,
- Martina Sůrová,
- Dana Šafka-Brožková,
- Saima Anwar,
- Judit Bene
- Published: April 17, 2015
- https://doi.org/10.1371/journal.pone.0124232