Nonsyndromic hearing loss caused by USH1G mutations: widening the USH1G disease spectrum.

Maria Oonk, Anne Marthe; van Huet, Ramon A C; Leijendeckers, Joop M; Oostrik, Jaap; Venselaar, Hanka; van Wijk, Erwin; Beynon, Andy; Kunst, Henricus P M; Hoyng, Carel B; Kremer, Hannie; Schraders, Margit; Pennings, Ronald J E

Maria Oonk, Anne Marthe; van Huet, Ramon A C; Leijendeckers, Joop M; Oostrik, Jaap; Venselaar, Hanka; van Wijk, Erwin; Beynon, Andy; Kunst, Henricus P M; Hoyng, Carel B; Kremer, Hannie; Schraders, Margit; Pennings, Ronald J E.

Affiliation

Maria Oonk AM; 1Department of Otorhinolaryngology, Hearing and Genes, Radboud University Medical Center, Nijmegen, The Netherlands; 2Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands; 3Department of Ophthalmology, Radboud University Medical Center, Nijmegen, The Netherlands; 4Nijmegen Centre for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands; 5Centre for Molecular and Biomolecular Informatics, Radboud Univers

Ear Hear ; 36(2): 205-11, 2015.

Article de En | MEDLINE | ID: mdl-25255398

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Surdité neurosensorielle / Protéines de tissu nerveux Limites: Female / Humans / Male Langue: En Journal: Ear Hear Année: 2015 Type de document: Article Pays de publication: États-Unis d'Amérique

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