- Title
- Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31
- Creators
- Steve D M Brown - MRC Mammalian Genetics Unit and UK Mouse Genome CentrePhilomena Mburu - MRC Mammalian Genetics Unit and UK Mouse Genome CentreDominique Weil - Unité de Génétique des Déficits Sensoriels, INSERM U587, Institut PasteurStéphane Blanchard - Unité de Génétique des Déficits Sensoriels, INSERM U587, Institut PasteurRoney S Coimbra - Unité de Génétique des Déficits Sensoriels, INSERM U587, Institut PasteurAziz El-Amraoui - Unité de Génétique des Déficits Sensoriels, INSERM U587, Institut PasteurAnabel Varela - MRC Mammalian Genetics Unit and UK Mouse Genome Centre Cancer Cell Biology, Imperial School Of Science, Technology and Medicine, Hammmersmith CampusAdam J Paige - MRC Mammalian Genetics Unit and UK Mouse Genome CentreRalph H Holme - MRC Institute of Hearing Research, University of NottinghamRachel E Hardisty - MRC Mammalian Genetics Unit and UK Mouse Genome CentreAndreas Rump - MetaGen Pharmaceuticals Gmbh Institute of Molecular Biotechnology, Department of Genome AnalysisJo Clay - MRC Mammalian Genetics Unit and UK Mouse Genome CentrePete Glenister - MRC Mammalian Genetics Unit and UK Mouse Genome CentreAndre Rosenthal - MetaGen Pharmaceuticals Gmbh Institute of Molecular Biotechnology, Department of Genome AnalysisKaren P Steel - MRC Institute of Hearing Research, University of NottinghamChristine Petit - Unité de Génétique des Déficits Sensoriels, INSERM U587, Institut PasteurMirna Mustapha - Unité de Génétique des Déficits Sensoriels, INSERM U587, Institut PasteurNick Parkinson - MRC Mammalian Genetics Unit and UK Mouse Genome CentreGonzalo Blanco - MRC Mammalian Genetics Unit and UK Mouse Genome CentreAnn-Marie Mallon - MRC Mammalian Genetics Unit and UK Mouse Genome CentreMike J Rogers - MRC Institute of Hearing Research, University of NottinghamXue Zhong Liu - Department of Otolaryngology, University of MiamiLee Moir - MRC Mammalian Genetics Unit and UK Mouse Genome CentreIsabelle Perfettini - Unité de Génétique des Déficits Sensoriels, INSERM U587, Institut Pasteur
- Publication Details
- Nature genetics, Vol.34(4), pp.421-428
- Academic Unit
- Miller School of Medicine; UMMG Department of Otolaryngology
- Language
- English
- Resource Type
- Journal article
- PMID
- 12833159
- Record Identifier
- 991031599552502976
Journal article
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31
Nature genetics, Vol.34(4), pp.421-428
2003-08
PMID: 12833159
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
- Genetics & Heredity
- ESI research areas
- Molecular Biology & Genetics
UN Sustainable Development Goals (SDGs)
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Source: InCites