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The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)

1996; Wiley; Volume: 19; Issue: 12 Linguagem: Inglês

10.1002/(sici)1097-4598(199612)19

1097-4598

Ichizo Nishino, Mikio Komatsu, Soichi Kodama, Satoshi Horai, Ikuya Nonaka, Yu-ichi Goto,

Metabolism and Genetic Disorders

Muscle & NerveVolume 19, Issue 12 p. 1603-1604 Short Report The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) Ichizo Nishino MD, Corresponding Author Ichizo Nishino MD Department of Ultrastructural Research, National Institute of Neuroscience (NCNP), National Center of Neurology and Psychiatry, Tokyo, JapanDepartment of Ultrastructural Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Kodaira, Tokyo, JapanSearch for more papers by this authorMikio Komatsu MD, Mikio Komatsu MD Himeji Red Cross Hospital, Hyogo, JapanSearch for more papers by this authorSoichi Kodama MD, Soichi Kodama MD Himeji Red Cross Hospital, Hyogo, JapanSearch for more papers by this authorSatoshi Horai MD, Satoshi Horai MD Department of Human Genetics, National Institute of Genetics, Mishima, JapanSearch for more papers by this authorIkuya Nonaka MD, Ikuya Nonaka MD Department of Ultrastructural Research, National Institute of Neuroscience (NCNP), National Center of Neurology and Psychiatry, Tokyo, Japan Department of Laboratory Medicine, National Center Hospital for Mental, Nervous and Muscular Disorders, NCNP, Tokyo, JapanSearch for more papers by this authorYu-Ichi Goto MD, Yu-Ichi Goto MD Department of Ultrastructural Research, National Institute of Neuroscience (NCNP), National Center of Neurology and Psychiatry, Tokyo, JapanSearch for more papers by this author Ichizo Nishino MD, Corresponding Author Ichizo Nishino MD Department of Ultrastructural Research, National Institute of Neuroscience (NCNP), National Center of Neurology and Psychiatry, Tokyo, JapanDepartment of Ultrastructural Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Kodaira, Tokyo, JapanSearch for more papers by this authorMikio Komatsu MD, Mikio Komatsu MD Himeji Red Cross Hospital, Hyogo, JapanSearch for more papers by this authorSoichi Kodama MD, Soichi Kodama MD Himeji Red Cross Hospital, Hyogo, JapanSearch for more papers by this authorSatoshi Horai MD, Satoshi Horai MD Department of Human Genetics, National Institute of Genetics, Mishima, JapanSearch for more papers by this authorIkuya Nonaka MD, Ikuya Nonaka MD Department of Ultrastructural Research, National Institute of Neuroscience (NCNP), National Center of Neurology and Psychiatry, Tokyo, Japan Department of Laboratory Medicine, National Center Hospital for Mental, Nervous and Muscular Disorders, NCNP, Tokyo, JapanSearch for more papers by this authorYu-Ichi Goto MD, Yu-Ichi Goto MD Department of Ultrastructural Research, National Institute of Neuroscience (NCNP), National Center of Neurology and Psychiatry, Tokyo, JapanSearch for more papers by this author First published: December 1996 https://doi.org/10.1002/(SICI)1097-4598(199612)19:12 3.0.CO;2-SCitations: 32AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL No abstract is available for this article.Citing Literature Volume19, Issue12December 1996Pages 1603-1604 RelatedInformation