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Epileptic Seizures in a Patient with Mitochondrial Myopathy, Encephalopathy, Laetic Acidosis and Strokelike Episodes (MELAS)

✍ Scribed by Ariyuki Hori; Akira Yoshioka; Satoshi Kataoka; Kei Furui; Katsuyuki Tsukada; Hiroshi Kosoegawa; ; Genjiro Hirose


Book ID
118708401
Publisher
John Wiley and Sons
Year
1989
Tongue
English
Weight
146 KB
Volume
43
Category
Article
ISSN
1323-1316

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The 3260 mutation in mitochondrial DNA c
✍ Ichizo Nishino; Mikio Komatsu; Soichi Kodama; Satoshi Horai; Ikuya Nonaka; Yu-Ic πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 248 KB

Maternally inherited myopathy and cardiomyopathy (MIMyCa) is one of the phenotypic subgroups of mitochondrial diseases. There are two reports of European families with MyMICa associated with an Ato-G transition at nucleotide (nt) 3260 in the mitochondrial tRNAkU(UUR) We have identified the 3260 mut