A Novel Point Mutation in the Mitochondrial tRNASer(UCN) Gene Detected in a Family with MERRF/MELAS Overlap Syndrome-Reference-Cited by-同舟云学术

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A Novel Point Mutation in the Mitochondrial tRNASer(UCN) Gene Detected in a Family with MERRF/MELAS Overlap Syndrome

Published:1995-09 Issue:1 Volume:214 Page:86-93
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Nakamura M.,Nakano S.,Goto Y.,Ozawa M.,Nagahama Y.,Fukuyama H.,Akiguchi I.,Kaji R.,Kimura J.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Cited by 111 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Functional analysis of the novel mitochondrial tRNA^Trp and tRNA^Ser(AGY) variants associated with type 2 diabetes mellitus;World Journal of Diabetes;2024-08-15

2. Development of mitochondrial gene-editing strategies and their potential applications in mitochondrial hereditary diseases: a review;Cytotherapy;2024-01

3. Mitochondrial DNA 3252A>G mutation presenting as MERRF/MELAS overlapping syndrome: A case report;Neurology Asia;2023-12

4. tRNA Dysregulation in Neurodevelopmental and Neurodegenerative Diseases;Annual Review of Cell and Developmental Biology;2023-10-16

5. The Mitochondrial tRNASer(UCN) Gene: A Novel m.7484A>G Mutation Associated with Mitochondrial Encephalomyopathy and Literature Review;Life;2023-02-16

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