Publisher
Springer Berlin Heidelberg
Reference14 articles.
1. Jacobs HT, Turnbull DM (2005) Nuclear genes and mitochondrial translation: a new class of genetic disease. Trends Genet 21: 312–314
2. Mauro S di, Davidzon G (2005) Mitochondrial DNA and disease. Ann Med 37: 222–232
3. Munnich A (2000) Defects of the respiratory chain. In: Fernandes J, Saudubray JM, Berghe G van den (eds) Inborn metabolic diseases, 3rd edn. Springer, Berlin Heidelberg New York Tokyo, pp 158–168
4. Niers L, Heuvel L van den, Trijbels F et al. (2003) Prerequisites and strategies for prenatal diagnosis of respiratory chain deficiency in chorionic villi. J Inherit Metab Dis 26: 647–658
5. Nyhan WL, Ozand PT (1998) The lactic acidemias. In: Nyhan WL, Ozand PT (eds) Atlas of metabolic diseases. Chapmann & Hall Medical, London, pp 259–320