A multicenter study on the prevalence and spectrum of mutations in the otoferlin gene (<i>OTOF</i>) in subjects with nonsyndromic hearing impairment and auditory neuropathy
Montserrat Rodríguez-Ballesteros(Centre for Biomedical Network Research on Rare Diseases), Ignacio del Castillo, Manuel Sainz-Quevedo(Instituto de Investigación Biosanitaria de Granada), José Moreno-Barral(Universidad Nacional de Córdoba), Pierangela Castorina, Carme Medá(Hospital de Sant Pau), Manuela Villamar(Hospital Universitario Ramón y Cajal), Marta Lucía Tamayo(Pontificia Universidad Javeriana), Carlos Curet(Universidad Nacional de Córdoba), Miguel A. Moreno‐Pelayo(Hospital Universitario Ramón y Cajal), Socorro Tedín(Complejo Hospitalario de Ourense), Constantino Morera(Hospital Universitari i Politècnic La Fe), Janine Smith(Children's Hospital at Westmead), Klemens Frei(Medical University of Vienna), Mirta Martín(Hospital Universitario Ramón y Cajal), Nancy Gélvez(Pontificia Universidad Javeriana), M. A. Gil Olarte(Pontificia Universidad Javeriana), Laura Cavallé(Hospital Universitari i Politècnic La Fe), Paola Primignani(Ospedale Maggiore), Christiane Völter(St. Elisabeth-Hospital Bochum), Raúl Reynoso(Universidad Nacional de Córdoba), Umberto Ambrosetti, Elena Gómez-Rosas(Centre for Biomedical Network Research on Rare Diseases), Edoardo Arslan(University of Padua), Felipe Moreno, Stefano Berrettini(University of Pisa), M. Cruz Tapia(Hospital Clínico San Carlos), Rosamaria Santarelli(University of Padua)
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