The optimized allotopic expression of ND1 or ND4 genes restores respiratory chain complex I activity in fibroblasts harboring mutations in these genes

Author:

Bonnet Crystel,Augustin Sébastien,Ellouze Sami,Bénit Paule,Bouaita Aicha,Rustin Pierre,Sahel José-Alain,Corral-Debrinski Marisol

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology

Reference47 articles.

1. Prevalence of mitochondrial DNA disease in adults;Schaefer;Ann. Neurol.,2008

2. Leber's hereditary optic neuropathy: a multifactorial disease;Yen;Prog. Retin. Eye Res.,2006

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

4. Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation;Howell;Am. J. Hum. Genet.,1991

5. An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy;Johns;Biochem. Biophys. Res. Commun.,1992

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