Diaphanous homolog 3 (Diap3) Overexpression Causes Progressive Hearing Loss and Inner Hair Cell Defects in a Transgenic Mouse Model of Human Deafness

Open Access

Peer-reviewed

Research Article

Cynthia J. Schoen,

Affiliations Neuroscience Program, University of Michigan Health System, Ann Arbor, Michigan, United States of America, Molecular and Behavioral Neuroscience Institute, University of Michigan Health System, Ann Arbor, Michigan, United States of America
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Margit Burmeister,

Affiliations Molecular and Behavioral Neuroscience Institute, University of Michigan Health System, Ann Arbor, Michigan, United States of America, Department of Human Genetics, University of Michigan Health System, Ann Arbor, Michigan, United States of America, Department of Psychiatry, University of Michigan Health System, Ann Arbor, Michigan, United States of America
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Marci M. Lesperance

* E-mail:lesperan@umich.edu

Affiliation Division of Pediatric Otolaryngology, Department of Otolaryngology-Head and Neck Surgery, University of Michigan Health System, Ann Arbor, Michigan, United States of America
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Deafness
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Mouse models
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Genetically modified animals
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Cochlea
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Hyperexpression techniques
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Synapses
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Organ of Corti
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Mammalian genomics
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