Investigation of Common Mitochondrial Point Mutations in Korea-Reference-Cited by-同舟云学术

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Investigation of Common Mitochondrial Point Mutations in Korea

Published:2004-04 Issue:1 Volume:1011 Page:339-344
ISSN:0077-8923
Container-title:Annals of the New York Academy of Sciences
language:en
Short-container-title:

Author:

KWON SEON-JOO,PARK SUNG-SUP,KIM JONG-MIN,AHN TAE-BEOM,KIM SEUNG HYUN,KIM JUHAN,LEE SUNG-HYUN,HA CHOONG-KUN,AHN MOO-YOUNG,JEON BEOM S.

Publisher

Wiley

Subject

History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1196/annals.1293.034/fullpdf

Reference15 articles.

1. Clinical features of MELAS and mitochondrial DNA mutations;Goto;Muscle Nerve,1995

2. A mitochondrial disorders: a proposal for consensus diagnostic criteria for infants and children;Wolf;Neurology,2002

3. Respiratory chain encephalomyopathies: a diagnostic classification;Walker;Eur. Neurol.,1996

4. Diagnostic criteria for respiratory chain disorders in adults and children;Bernier;Neurology,2002

5. Does the patient have a mitochondrial encephalopathy;DiMauro;J. Child Neurol.,1999

Cited by 3 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. Identification of causative mutations in patients with Leigh syndrome and MERRF by mitochondrial DNA-targeted next-generation sequencing;Journal of Genetic Medicine;2015-12-31

2. Retrospective assessment of the most common mitochondrial DNA mutations in a large Hungarian cohort of suspect mitochondrial cases;Mitochondrial DNA;2014-01-17

3. Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases;Experimental and Molecular Medicine;2010

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