MELAS syndrome with m.4450 G > A mutation in mitochondrial tRNAMet gene.
Kuwajima M, Goto M, Kurane K, Shimbo H, Omika N, Jimbo EF, Muramatsu K, Tajika M, Shimura M, Murayama K, Kurosawa K, Yamagata T, Osaka H.
Kuwajima M, et al. Among authors: kurane k.
Brain Dev. 2019 May;41(5):465-469. doi: 10.1016/j.braindev.2019.01.006. Epub 2019 Feb 7.
Brain Dev. 2019.
PMID: 30739820