The mitochondrial A3243G mutation involves the peripheral vestibule as well as the cochlea
Author:
Publisher
Wiley
Subject
Otorhinolaryngology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/lary.21879/fullpdf
Reference21 articles.
1. Diseases of mitochondrial DNA;Wallace;Annu Rev Biochem,1992
2. Mitochondrial deafness;Kokotas;Clin Genet,2007
3. Non-Mendelian mitochondrial inheritance as a cause of progressive genetic sensorineural hearing loss;Gold;Int J Pediatr Otorhinolaryngol,1994
4. Auditory findings in patients with maternally inherited diabetes and deafness harboring a point mutation in the mitochondrial transfer RNALeu (UUR) gene;Yamasoba;Laryngoscope,1996
5. Cochlear histopathology associated with mitochondrial transfer RNALeu (UUR) gene mutation;Yamasoba;Neurology,1999
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