Mitochondrial tRNA mutations associated with deafness
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Molecular Medicine
Reference93 articles.
1. The pathogenic m.3243A>T mitochondrial DNA mutation is associated with a variable neurological phenotype;Alston;Neuromuscul. Disord.,2010
2. Sequence and organization of the human mitochondrial genome;Anderson;Nature,1981
3. Sporadic mitochondrial myopathy due to a new mutation in the mitochondrial tRNASer(UCN) gene;Bidooki;Neuromuscul. Disord.,2004
4. Rapidly progressive neurodegeneration in a case with the 7472insC mutation and the A7472C polymorphism in the mtDNA tRNASer(UCN) gene;Cardaioli;Neuromuscul. Disord.,2006
5. A novel heteroplasmic tRNASer(UCN) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing loss;Cardaioli;Neuromuscul. Disord.,2007
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