Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease

Author:

Pello Rosa,Martín Miguel A.,Carelli Valerio,Nijtmans Leo G.,Achilli Alessandro,Pala Maria,Torroni Antonio,Gómez-Durán Aurora,Ruiz-Pesini Eduardo,Martinuzzi Andrea,Smeitink Jan A.,Arenas Joaquín,Ugalde Cristina

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference38 articles.

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2. Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation;Harding;Am. J. Hum. Genet.,1995

3. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy;Wallace;Science,1988

4. Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage;Brown;Am. J. Hum. Genet.,1997

5. Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease;Hofmann;Hum. Mol. Genet.,1997

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