A point mutation in the mitochondrial tRNALeu(UUR) gene in melas (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)-Reference-Cited by-同舟云学术

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A point mutation in the mitochondrial tRNALeu(UUR) gene in melas (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)

Published:1990-12 Issue:3 Volume:173 Page:816-822
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Kobayashi Yoko,Momoi Mariko Y.,Tominaga Kaoru,Momoi Takashi,Nihei Kenji,Yanagisawa Masayoshi,Kagawa Yasuo,Ohta Shigeo

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference30 articles.

1. Mitochondrial myopathies

2. THE CLINICAL FEATURES OF MITOCHONDRIAL MYOPATHY

3. Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities): Disease entity or a syndrome?

4. Progressive cytochromec oxidase deficiency in a case of earns-sayre syndrome: Morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissues

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

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