Abstract
PCR amplification (followed by mutation scanning or direct sequencing) is a technique widely used in mutation detection and molecular studies of disease-causing genes, such as ARX. PCR amplification of high GC-rich regions encounters difficulties using conventional PCR procedures. Here, we present the strategies to amplify and sequence these GC-rich regions for the purposes of mutation screening and other molecular analyses.
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Acknowledgments
This work was supported by grants from the National Health and Medical Research Council of Australia (Project Grant 1002732 to C.S.; Principle Research Fellowship 508043 to J.G.) and MS McLeod Foundation Fellowship to C.S. and postgraduate scholarship to M.H.T.
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Tan, M.H., Gécz, J., Shoubridge, C. (2013). PCR Amplification and Sequence Analysis of GC-Rich Sequences: Aristaless-Related Homeobox Example. In: Hatters, D., Hannan, A. (eds) Tandem Repeats in Genes, Proteins, and Disease. Methods in Molecular Biology, vol 1017. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-62703-438-8_8
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DOI: https://doi.org/10.1007/978-1-62703-438-8_8
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