Mitochondrial leucine tRNA mutation in a mitochondrial encephalomyopathy

Author:

Ino Hidekazu,Tanaka Masashi,Ohno Kinji,Hattori Kazuki,Ikebe Shin-Ichiro,Sano Tadashi,Ozawa Takayuki,Ichiki Takashi,Yashi MasanoriKoba,Wada Yoshiro

Publisher

Elsevier BV

Subject

General Medicine

Reference6 articles.

1. Multiple populations of deleted mitochondrial DNA detected by a novel gene amplification method;Sato;Biochem Biophys Res Commun,1989

2. Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy;Ozawa;Biochem Biophys Res Commun,1988

3. Myotomc epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation;Shoffner;Cell,1990

4. A common mitochondrial DNA mutation in the t-RNALys of patients with myoclonus epilepsy associated with ragged-red fibers;Yoneda;Biochem Int,1990

5. Deficiency of subunits of Complex I and mitochondrial encephalomyopathy;Ichiki;Ann Neurol,1988

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