Auditory Findings in Patients with Maternally Inherited Diabetes and Deafness Harboring a Point Mutation in the Mitochondrial Transfer RNALeu (UUR)Gene-Reference-Cited by-同舟云学术

Auditory Findings in Patients with Maternally Inherited Diabetes and Deafness Harboring a Point Mutation in the Mitochondrial Transfer RNALeu (UUR)Gene

Published:1996-01 Issue:1 Volume:106 Page:49-53
ISSN:0023-852X
Container-title:The Laryngoscope
language:en
Short-container-title:Laryngoscope

Author:

Yamasoba Tatsuya,Oka Yoshitomo,Tsukuda Katsunori,Nakamura Masaichi,Kaga Kimitaka

Publisher

Wiley

Subject

Otorhinolaryngology

Reference26 articles.

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2. Clinicopathological classification of mitochondrial myopathies;Fukuhara;Neurol Med Chir (Tokyo),1986

3. Audiological findings in a family with mitochondrial disorder;Elverland;Am J Otol,1991

4. Histopathological features of the inner ear associated with Kearns-Sayre syndrome;Lindsay;Arch Otolaryngol Head Neck Surg,1976

5. Familiäre Neural Mitochondriale Schwerhörigkeit;Marangos;HNO,1990

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