Quantitation of mitochondrial DNA carrying tRNALys mutation in MERRF patients

Author:

Tanno Yoshinori,Yoneda Makoto,Nonaka Ikuya,Tanaka Keiko,Miyatake Tadashi,Tsuji Shoji

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Cited by 51 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. Improving post-natal detection of mitochondrial DNA mutations;Expert Review of Molecular Diagnostics;2020-09-20

2. MERRF Classification: Implications for Diagnosis and Clinical Trials;Pediatric Neurology;2018-03

3. Pathophysiology of Cardiomyopathies;Fetal and Neonatal Physiology;2017

4. When should MERRF (myoclonus epilepsy associated with ragged-red fibers) be the diagnosis?;Arquivos de Neuro-Psiquiatria;2014-10

5. Myoclonic epilepsy and ragged red fiber (MERRF) disease;Atlas of Inherited Metabolic Diseases 3E;2011-12-30

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