A combination of two truncating mutations in USH2A causes more severe and progressive hearing impairment in Usher syndrome type IIa

作者：Bas P. Hartel, Maria Löfgren, Patrick L. M. Huygen, Iris Guchelaar, Nicole Lo-A-Njoe Kort, Mehdi Sadeghi, Erwin van Wijk, Lisbeth Tranebjærg, Hannie Kremer, William J. Kimberling, Cor W. R. J. Cremers, Claes Möller, Ronald J. E. Pennings · 发表于：Hearing Research · 年份：2016 · DOI：10.1016/j.heares.2016.06.008 · 被引用次数：64 · 研究领域：Hearing, Cochlea, Tinnitus, Genetics、Vestibular and auditory disorders、Hearing Loss and Rehabilitation