Detection of common disease-causing mutations in mitochondrial DNA (mitochondrial encephalomyopathy, lactic acidosis with stroke-like episodes MTTL1 3243 A>G and myoclonic epilepsy associated with ragged-red fibers MTTK 8344A>G) by real-time polymerase chain reaction.
The Journal of molecular diagnostics : JMD 2006 May 8 (2): 277-81.
Fan Hongxin, Civalier Chris, Booker Jessica K, Gulley Margaret L, Prior Thomas W, Farber Rosann
Clinical features of A3243G mitochondrial tRNA mutation.
Brain & development 2004 Oct 26 (7): 459-62.
Chae Jong Hee, Hwang Hee, Lim Byung Chan, Cheong Hae Il, Hwang Yong Seung, Kim Ki Joo