CHD7 Deficiency in “Looper”, a New Mouse Model of CHARGE Syndrome, Results in Ossicle Malformation, Otosclerosis and Hearing Impairment

• Jacqueline M. Ogier,

  Affiliation Murdoch Childrens Research Institute, Parkville, Victoria, Australia

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• Marina R. Carpinelli,

  Affiliations Murdoch Childrens Research Institute, Parkville, Victoria, Australia, The HEARing Cooperative Research Centre, Parkville, Victoria, Australia, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia, Department of Medical Biology, University of Melbourne, Parkville, Victoria, Australia

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• Benedicta D. Arhatari,

  Affiliation ARC Centre of Excellence for Coherent X-ray Science, Department of Physics, La Trobe University, Bundoora, Victoria, Australia

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• R. C. Andrew Symons,

  Affiliation Department of Ophthalmology, Royal Melbourne Hospital, Parkville, Victoria, Australia

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• Benjamin T. Kile,

  Affiliations Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia, Department of Medical Biology, University of Melbourne, Parkville, Victoria, Australia, Department of Genetics, University of Melbourne, Parkville, Victoria, Australia

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• Rachel A. Burt

  * E-mail: rachel.burt@mcri.edu.au

  Affiliations Murdoch Childrens Research Institute, Parkville, Victoria, Australia, The HEARing Cooperative Research Centre, Parkville, Victoria, Australia, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia, Department of Genetics, University of Melbourne, Parkville, Victoria, Australia, Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia

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