David C. Kohrman
University of Michigan–Ann Arbor(US)University of Michigan(US)Kresge Eye Institute(US)Michigan Medicine(US)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Hearing Loss and Rehabilitation, RNA and protein synthesis mechanisms, Vestibular and auditory disorders, Ion channel regulation and function
Most-Cited Works
- → Mutation of a new sodium channel gene, Scn8a, in the mouse mutant ‘motor endplate disease’(1995)311 cited
- → Mutations in a Novel Gene, TMIE, Are Associated with Hearing Loss Linked to the DFNB6 Locus(2002)144 cited
- → Mutation Detection in the and Alleles of the Sodium Channel(1996)142 cited
- → A Missense Mutation in the Sodium Channel Scn8a Is Responsible for Cerebellar Ataxia in the Mouse Mutantjolting(1996)133 cited
- → Hidden Hearing Loss: A Disorder with Multiple Etiologies and Mechanisms(2019)127 cited
- → Exon Organization, Coding Sequence, Physical Mapping, and Polymorphic Intragenic Markers for the Human Neuronal Sodium Channel GeneSCN8A(1998)93 cited