Analysis of Common Mitochondrial DNA Mutations by Allele-Specific Oligonucleotide and Southern Blot Hybridization-Reference-Cited by-同舟云学术

Analysis of Common Mitochondrial DNA Mutations by Allele-Specific Oligonucleotide and Southern Blot Hybridization

Published:2011-12-20 Issue: Volume: Page:259-279
ISSN:1064-3745
Container-title:Methods in Molecular Biology
language:
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Author:

Tang Sha,Halberg Michelle C.,Floyd Kristen C.,Wang Jing

Publisher

Humana Press

Link

http://link.springer.com/content/pdf/10.1007/978-1-61779-504-6_18.pdf

Reference12 articles.

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3. Tatuch Y, Christodoulou J, Feigenbaum A, Clarke JT, Wherret J, Smith C, et al. Heteroplasmic mtDNA mutation (T—G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high. Am J Hum Genet. 1992 Apr;50(4):852–8.

4. Wong LJ. Comprehensive molecular diagnosis of mitochondrial disorders: qualitative and quantitative approach. Ann N Y Acad Sci. 2004 Apr;1011:246–58.

5. Wong LJ, Senadheera D. Direct detection of multiple point mutations in mitochondrial DNA. Clin Chem. 1997 Oct;43(10):1857–61.

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