Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation

By Guan M-X.  

Human Molecular Genetics, Vol. 10, Iss. 6, 2001-03 ,pp. : 573-580

Oxford University Press

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A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction

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Oxford University Press

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Molecular Phenotype of a Human Lymphoblastoid Cell-line Homoplasmic for the np 7445 Deafness-associated Mitochondrial Mutation

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Human Molecular Genetics, Vol. 6, Iss. 3, 1997-01 ,pp. : 443-449

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Biochemical Evidence for Nuclear Gene Involvement in Phenotype of Non-Syndromic Deafness Associated with Mitochondrial 12S rRNA Mutation

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Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

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