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High Prevalence of the COII/tRNALysIntergenic 9-bp Deletion in Mitochondrial DNA of Taiwanese Patients with MELAS or MERRF Syndrome

  • Published:2005-05 Issue:1 Volume:1042 Page:82-87
  • ISSN:0077-8923
  • Container-title:Annals of the New York Academy of Sciences
  • language:en
  • Short-container-title:

Author:

LIU CHIN-SAN,CHENG WEN-LING,CHEN YI-YUN,MA YI-SHING,PANG CHENG-YOONG,WEI YAU-HUEI

Publisher

Wiley

Subject

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

Reference17 articles.

1. Length mutations in human mitochondrial DNA;Cann;Genetics,1983

2. Length mutations in human mitochondrial DNA: direct sequencing of enzymatically amplified DNA;Wrischnik;Nucleic Acids Res.,1987

3. Molecular epidemiologic study of mitochondrial DNA mutations in patients with mitochondrial diseases in Taiwan;Pang;J. Formos. Med. Assoc.,1999

4. MELAS syndrome with mitochondrial tRNALeu (UUR) gene mutation in a Chinese family;Huang;J. Neurol. Neurosurg. Psychiatry,1994

5. Evolutionary history of the mtDNA 9-bp deletion in Chinese populations and its relevance to the peopling of east and southeast Asia;Yao;Hum. Genet.,2000

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