Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)-Reference-Cited by-同舟云学术

Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)

Published:1991-01 Issue:2 Volume:174 Page:861-868
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Tanaka Masashi,Ino Hidekazu,Ohno Kinji,Ohbayashi Toshihiro,Ikebe Shin-ichiro,Sano Tadashi,Ichiki Takashi,Kobayashi Masanori,Wada Yoshiro,Ozawa Takayuki

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference28 articles.

1. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

2. A mitochondrial encephalomyopathy with cardiomyopathy

3. Deficiency of subunits in heart mitochondrial NADH-ubiquinone oxidoreductase of a patient with mitochondrial encephalomyopathy and cardiomyopathy

4. Deficiency of subunits of complex I and mitochondrial encephalomyopathy

5. Disproportionate Deficiency of Iron-Sulfur Clusters and Subunits of Complex I in Mitochondrial Encephalomyopathy

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