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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Spontaneous event of mitochondrial DNA mutation, A3243G, found in a family of identical twins

By Harihara Shinji  

Mitochondrial DNA, Vol. 24, Iss. 2, 2013-04 ,pp. : 158-162

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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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Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation

By Giordano C.   Pallotti F.   Walker W.F.   Checcarelli N.   Musumeci O.   Santorelli F.   d'Amati G.   Schon E.A.   DiMauro S.   Hirano M.   Davidson M.M.  

Biochemical and Biophysical Research Communications, Vol. 293, Iss. 1, 2002-04 ,pp. : 521-529

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

By Kameoka K.   Isotani H.   Tanaka K.   Azukari K.   Fujimura Y.   Shiota Y.   Sasaki E.   Majima M.   Furukawa K.   Haginomori S.   Kitaoka H.   Ohsawa N.  

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

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