Nonsense Mutations in SMPX, Encoding a Protein Responsive to Physical Force, Result in X-Chromosomal Hearing Loss
Antje K. Huebner(Jena University Hospital), Ingo Kurth(Universität Hamburg), Janine Altmüller(Max Delbrück Center), Luis A. Aguirre(Centre for Biomedical Network Research on Rare Diseases), Hölger Thiele(Leipzig Heart Institute), Eva M. Wicklein(Universität Hamburg), A Maak(Jena University Hospital), Florian Wagner(Atlas Biolabs (Germany)), Antonio Viñuela(Centre for Biomedical Network Research on Rare Diseases), Gudrun Nürnberg(University of Cologne), Peter Frommolt(University of Cologne), Andreas Gal(Universität Hamburg), Ignacio del Castillo, Peter Nürnberg(University of Cologne), H. Maier(Medizinische Hochschule Hannover), Isabella Rau(Universität Hamburg), Felipe Moreno, Christian A. Hübner(University of Wuppertal), Marta Gandía(Centre for Biomedical Network Research on Rare Diseases), Sebastian Gießelmann(Jena University Hospital)
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