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Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairment

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Year: 2013
Type: article
Study design: Case Report
Source: Gene
DOI: 10.1016/j.gene.2013.06.044
Authors: C. Bonnet, M. Louha, N. Loundon, N. Michalski, E. Verpy, L. Smagghe, J.-P. Hardelin, I. Rouillon, L. Jonard, R. Couderc, S. Gherbi, E.N. Garabedian, F. Denoyelle, C. Petit, S. Marlin
Institutions: Institut de la Vision, Inserm, Université Pierre-et-Marie-Curie, Hôpital Armand-Trousseau, Assistance Publique – Hôpitaux de Paris, Institut Pasteur, Institut de l'Audition, Collège de France
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
OpenAlex ID: W2019225859
FWCI: 2.282
Cites: 15
Cited by: 29
Related to: 10
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