Author:
Lin Virginia W.,Pavlakis Steven G.
Publisher
Springer International Publishing
Reference112 articles.
1. Pavlakis SG, Phillips PC, DiMauro S, De Vivo DC, Rowland LP. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome. Ann Neurol. 1984;16(4):481–8.
2. Sproule DM, Kaufmann P. Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome. Ann N Y Acad Sci. 2008;1142:133–58.
3. Schon EA. The mitochondrial genome. In: Rosenberg RPS, DiMauro S, Barchi R, Nestler E, editors. The molecular and genetic basis of neurologic and psychiatric disease. 3rd ed. Philadelphia: Butterworth-Heinemann; 2003. p. 179–88.
4. Anderson S, Bankier AT, Barrel BG. Sequence and organization of the human mitochondrial genome. Nature. 1981;290:457–65.
5. Wong JL. Pathogenic mitochondrial DNA mutations in protein-coding genes. Muscle Nerve. 2007;36(3):279–93.