Síndrome de diabetes de herencia materna y sordera
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology
Reference9 articles.
1. Prevalence of mitochondrial gene mutations among hearing impaired patients;Usami;J Med Genet,2000
2. Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion;Ballinger;Nat Genet,1992
3. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome;Pavlakis;Ann Neurol,1984
4. Areview of cochlear implantation in mitochondrial sensorineural hearing loss;Sinnathuray;Otol Neurotol,2003
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Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A>G and the ND1 m.3308T>C mutations associated with multiple mitochondrial deletions;Biochemical and Biophysical Research Communications;2013-02
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