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

By Reid Fiona M.   Rovio Anja   Holt Ian J.   Jacobs Howard T.  

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

Oxford University Press

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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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Complex I deficiency is Associated with 3243G:C Mitochondrial DNA in Osteosarcoma Cell Cybrids

By Dunbar D. R.   Moonie P. A.   Zeviani M.   Holt I. J.  

Human Molecular Genetics, Vol. 5, Iss. 1, 1996-01 ,pp. : 123-129

Oxford University Press

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

By Guan Min-Xin   Fischel-Ghodsian Nathan   Attardi Giuseppe  

Human Molecular Genetics, Vol. 5, Iss. 7, 1996-01 ,pp. : 963-971

Oxford University Press

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Suppression of a mitochondrial tRNA gene mutation phenotype associated with changes in the nuclear background

By Hao Huiling  

Human Molecular Genetics, Vol. 8, Iss. 6, 1999-06 ,pp. : 1117-1124

Oxford University Press

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