Work

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

Year: 2016

Type: article

Study design: Observational Study

Source: Hearing Research

DOI: 10.1016/j.heares.2016.06.008

Authors: Bas P. Hartel, Maria Löfgren, Patrick L.M. Huygen, Iris Guchelaar, Nicole Lo-A-Njoe Kort, Andre M. Sadeghi, Erwin van Wijk, Lisbeth Tranebjærg, Hannie Kremer, William J. Kimberling, Cor W.R.J. Cremers, Claes Möller, Ronald J.E. Pennings

Institutions: Radboud University Medical Center, Radboud Institute for Health Sciences, Örebro University, Örebro University Hospital, University of Gothenburg, Radboud University Nijmegen, Radboud Institute for Molecular Life Sciences, Donders Institute for Brain, Cognition and Behaviour, University of Copenhagen, Bispebjerg Hospital, Rigshospitalet, University of Iowa

Language: English

Topic: Hearing, Cochlea, Tinnitus, Genetics

Subfield: Sensory Systems

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: ZonMw, Nederlandse Organisatie voor Wetenschappelijk Onderzoek

Awards: G5473850642, G7172780514, G937998289

OpenAlex ID: W2439102966

FWCI: 2.84

Cites: 42

Cited by: 58

Related to: 10