- Title
- Similar phenotypes caused by mutations in OTOG and OTOGL
- Creators
- Anne M.M Oonk - Department of Otorhinolaryngology, Hearing & Genes, Radboud University Nijmegen Medical Centre, Nijmegen, the NetherlandsJoop M Leijendeckers - Department of Otorhinolaryngology, Hearing & Genes, Radboud University Nijmegen Medical Centre, Nijmegen, the NetherlandsPatrick L.M Huygen - Department of Otorhinolaryngology, Hearing & Genes, Radboud University Nijmegen Medical Centre, Nijmegen, the NetherlandsMargit Schraders - Department of Otorhinolaryngology, Hearing & Genes, Radboud University Nijmegen Medical Centre, Nijmegen, the NetherlandsMiguel del Campo - Unidad de Genética Clínica, Programa de Medicina Molecular y Genética, Hospital Universitario Vall d'Hebron, Barcelona, SpainIgnacio del Castillo - Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Madrid, SpainMustafa Tekin - John P. Hussman Institute for Human Genomics, University of Miami, Miami, USAIlse Feenstra - Department of Human Genetics, Radboud University Nijmegen Medical Centre, the NetherlandsAndy J Beynon - Department of Otorhinolaryngology, Hearing & Genes, Radboud University Nijmegen Medical Centre, Nijmegen, the NetherlandsHenricus P.M Kunst - Department of Otorhinolaryngology, Hearing & Genes, Radboud University Nijmegen Medical Centre, Nijmegen, the NetherlandsAd F.M Snik - Department of Otorhinolaryngology, Hearing & Genes, Radboud University Nijmegen Medical Centre, Nijmegen, the NetherlandsHannie Kremer - Department of Otorhinolaryngology, Hearing & Genes, Radboud University Nijmegen Medical Centre, Nijmegen, the NetherlandsRonald J.C Admiraal - Department of Otorhinolaryngology, Hearing & Genes, Radboud University Nijmegen Medical Centre, Nijmegen, the NetherlandsRonald J.E Pennings - Department of Otorhinolaryngology, Hearing & Genes, Radboud University Nijmegen Medical Centre, Nijmegen, the Netherlands
- Publication Details
- Ear and hearing, Vol.35(3), pp.e84-e91
- Academic Unit
- Miller School of Medicine; UMMG Dept of Human Genetics - Clinical and Translational Genetics; UMMG Dept of Human Genetics (Dr. John T. Macdonald Foundation)
- Language
- English
- Resource Type
- Journal article
- PMID
- 24378291
- PMCID
- PMC3999258
- Record Identifier
- 991031576387602976
Journal article
Similar phenotypes caused by mutations in OTOG and OTOGL
Ear and hearing, Vol.35(3), pp.e84-e91
2014
PMCID: PMC3999258
PMID: 24378291
Metrics
8 Record Views
InCites Highlights
These are selected metrics from InCites Benchmarking & Analytics tool, related to this output
- Collaboration types
- Domestic collaboration
- International collaboration
- Citation topics
- 1 Clinical & Life Sciences
- 1.150 Hearing Loss
- 1.150.421 Cochlea
- Web Of Science research areas
- Audiology & Speech-language Pathology
- Otorhinolaryngology
- ESI research areas
- Clinical Medicine
UN Sustainable Development Goals (SDGs)
This output has contributed to the advancement of the following goals:
Source: InCites