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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Molecular phenotype of the np 7472 deafness-associated mitochondrial mutation in osteosarcoma cell cybrids

By Toompuu Marina  

Human Molecular Genetics, Vol. 8, Iss. 12, 1999-11 ,pp. : 2275-2283

Oxford University Press

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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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A2144G Is the Main Mutation in the 23S rRNA Gene of Helicobacter pylori Associated with Clarithromycin Resistance

By Momynaliev K.   Selezneva O.   Kozlova A.   Vereshchagin V.   Il'ina E.   Govorun V.  

Russian Journal of Genetics, Vol. 41, Iss. 10, 2005-10 ,pp. : 1095-1100

MAIK Nauka/Interperiodica

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