Application of Cochlear Implant for Two Cases of Maternally Inherited Diabetes and Deafness
Author:
Affiliation:
1. Department of Otolaryngology, Ichinomiyanishi Hospital
2. Department of Otorhinolaryngology, Gifu University Graduate School of Medicine
Publisher
The Society of Practical Otolaryngology
Subject
Otorhinolaryngology
Link
https://www.jstage.jst.go.jp/article/jibirinsuppl/152/0/152_8/_pdf
Reference15 articles.
1. 1) van den Ouweland JM, Lemkes HH, Ruitenbeek W, et al. : Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness. Nat Genet 1: 368–371, 1992.
2. 2) Murphy R, Turnbull DM, Walker M, et al. : Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation. Diabet Med 25: 383–399, 2008.
3. 3) Chinnery PF, Elliott C, Green GR, et al. : The spectrum of hearing loss due to mitochondrial DNA defects. Brain 123: 82–92, 2000.
4. 4) Deschauer M, Müller T, Wieser T, et al. : Hearing impairment is common in various phenotypes of the mitochondrial DNA A3243G mutation. Arch Neurol 58: 1885–1888, 2001.
5. 5) Usami S, Abe S, Akita J, et al. : Prevalence of mitochondrial gene mutations among hearing impaired patients. J Med Genet 37: 38–40, 2000.
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