Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear–mitochondrial interaction
- 1 May 2003
- journal article
- review article
- Published by Elsevier in Trends in Genetics
- Vol. 19 (5) , 257-262
- https://doi.org/10.1016/s0168-9525(03)00072-6
Abstract
No abstract availableKeywords
This publication has 42 references indexed in Scilit:
- Respiratory function in cybrid cell lines carrying European mtDNA haplogroups: implications for Leber's hereditary optic neuropathyBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 2002
- Chapter 4 Leber's Hereditary Optic NeuropathyPublished by Elsevier ,2002
- Mitochondrial DNA mutations in human diseaseAmerican Journal of Medical Genetics, 2001
- Mitochondrial defects and hearing lossCellular and Molecular Life Sciences, 2000
- The A1555G Mutation in the 12S rRNA Gene of Human mtDNA: Recurrent Origins and Founder Events in Families Affected by Sensorineural DeafnessAmerican Journal of Human Genetics, 1999
- Mitochondrial Diseases in Man and MouseScience, 1999
- Coexistence of mitochondrial DNA and beta myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failureHeart, 1998
- Low-Penetrance Branches in Matrilineal Pedigrees with Leber Hereditary Optic NeuropathyAmerican Journal of Human Genetics, 1998
- Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafnessNature Genetics, 1993
- Sequence and organization of the human mitochondrial genomeNature, 1981