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Pregnancy with mitochondrial encephalopathy, lactic acidosis, and strokelike episodes syndrome

โœ Scribed by Oormila P Kovilam; William Cahill; Tariq A Siddiqi


Book ID
117193183
Publisher
Lippincott Williams and Wilkins
Year
1999
Tongue
English
Weight
118 KB
Volume
93
Category
Article
ISSN
0029-7844

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The 3260 mutation in mitochondrial DNA c
โœ Ichizo Nishino; Mikio Komatsu; Soichi Kodama; Satoshi Horai; Ikuya Nonaka; Yu-Ic ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 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