Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases-Reference-Cited by-同舟云学术

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Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases

Published:2010 Issue:6 Volume:42 Page:446
ISSN:1226-3613
Container-title:Experimental and Molecular Medicine
language:en
Short-container-title:Exp Mol Med

Author:

Choi Byung-Ok¹,Hwang Jung Hee²³,Cho Eun Min²,Jeong Eun Hye¹,Hyun Young Se²,Jeon Hyeon Jeong²,Seong Ki Min²³,Cho Nam Soo³,Chung Ki Wha²

Affiliation:

1. Department of Neurology, Ewha Womans University, School of Medicine, Ewha Medical Research Institute, Seoul 158-710, Korea.

2. Department of Biological Science, Kongju National University, Gongju 314-701, Korea.

3. DNA Analysis Division, National Institute of Scientific Investigation, Seoul 158-097, Korea.

Publisher

Springer Science and Business Media LLC

Subject

Clinical Biochemistry,Molecular Biology,Molecular Medicine,Biochemistry

Reference37 articles.

1. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

2. Investigation of the Role of Mitochondrial DNA in Multiple Sclerosis Susceptibility

3. Diagnostic criteria for respiratory chain disorders in adults and children

4. Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear–mitochondrial interaction

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1. Mitochondrial myopathies diagnosed in adulthood: clinico-genetic spectrum and long-term outcomes;Brain Communications;2024

2. Independent origin for m.3243A>G mitochondrial mutation in three Venezuelan cases of MELAS syndrome;Clinical Biochemistry;2022-11

3. A Systematic Review of the Impact of Mitochondrial Variations on Male Infertility;Genes;2022-06-30

4. Diagnosis of primary mitochondrial disorders -Emphasis on myopathological aspects;Mitochondrion;2021-11

5. No MELAS syndrome without heteroplasmy levels or multisystem examination;NEUROLOGIA;2020

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