A Case of a De Novo A3243G Mutation in Mitochondrial DNA in a Patient with Diabetes and Deafness

By Maassen J.A.   Biberoglu S.   Hart L.M. 't   Bakker E.   de Knijff P.  

Archives of Physiology and Biochemistry, Vol. 110, Iss. 3, 2002-07 ,pp. : 186-188

Informa Healthcare

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Novel Mitochondrial DNA Mutation in tRNALys (8296A -< G) Associated with Diabetes

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Biochemical and Biophysical Research Communications, Vol. 245, Iss. 2, 1998-04 ,pp. : 523-527

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Accumulation of Somatic Nucleotide Substitutions in Mitochondrial DNA Associated with the 3243 A-to-G tRNA Leu(UUR) Mutation in Encephalomyopathy and Cardiomyopathy

By Kovalenko S.A.   Tanaka M.   Yoneda M.   Iakovlev A.F.   Ozawa T.  

Biochemical and Biophysical Research Communications, Vol. 222, Iss. 2, 1996-05 ,pp. : 201-207

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Biochemical characterization of the mitochondrial tRNA Ser(UCN) T7511C mutation associated with nonsyndromic deafness

By Li Xiaoming  

Nucleic Acids Research, Vol. 32, Iss. 3, 2004-02 ,pp. : 867-877

Oxford University Press

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Heterogeneity of six children and their mothers with mitochondrial DNA 3243 A>G mutation

By Ma Yan-Yan  

Mitochondrial DNA, Vol. 24, Iss. 3, 2013-06 ,pp. : 297-302

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