Defects of intergenomic communication: autosomal disorders that cause multiple deletions and depletion of mitochondrial DNA

Author:

Hirano Michio,Marti Ramon,Ferreiro-Barros Claudia,Vilà Maya R,Tadesse Saba,Nishigaki Yutaka,Nishino Ichizo,Vu Tuan H

Publisher

Elsevier BV

Subject

Cell Biology,Developmental Biology

Reference93 articles.

1. An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region;Zeviani;Nature,1989

2. MtDNA depletion with variable tissue expression: A novel genetic abnormality in mitochondrial diseases;Moraes;Am J Hum Genet,1991

3. Sequence and organization of the human mitochondrial genome;Anderson;Nature,1981

4. Mitochondrial DNA maintenance in vertebrates;Shadel;Ann Rev Biochem,1997

5. The mitochondrial genome: structure, transcription and translation;Taanman;Biochim Biophys Acta,1999

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