Identification of a Novel WFS1 Mutation Using the Whole Exome Sequencing in an Iranian Pedigree with Autosomal Dominant Hearing Loss

por Mohammadi-asl, Javad, Saki, Nader, Dehdashtiyan, Masoud, Neissi, Mostafa, Ghanbari Mardasi, Farideh
Publicado 2021