The AGG interruption pattern within the CGG repeat of the FMR1 gene among Taiwanese population
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://link.springer.com/content/pdf/10.1007/s12041-008-0043-1.pdf
Reference15 articles.
1. Angeli C. B., Capelli L. P., Auricchio M. T., Leal-Mesquita E. R., Ribeiro-dos-Santos K., Ferrari I. et al. 2005 AGG interspersion patterns in the CGG repeat of the FMR1 gene and linked DSX548/FRAXACA1 haplotypes in Brazilian populations. Am. J. Med. Genet. 132, 210–214.
2. Chen S. H., Schoof J., Buroker N. E. and Scott C. R. 1997 The identification of a (CGG)6AGG insertion within the CGG repeat of the FMR1 gene in Asians. Hum. Genet. 99, 793–795.
3. Crawford D. C., Schwartz C. E., Meadows K. L., Newman J. L., Taft L. F., Gunter C. et al. 2000 Survey of the fragile X syndrome CGG repeat and the short-tandem repeat and single-nucleotidepolymorphism haplotypes in an African-American population. Am. J. Hum. Genet. 66, 480–493.
4. Eichler E. E., Hammond H. A., Macpherson J. N., Ward P. A. and Nelson D. L. 1995 Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions. Hum. Mol. Genet. 4, 2199–2208.
5. Entezam A., Biacsi R., Orrison B., Saha T., Hoffman G. E., Grabczyk E. et al. 2007 Regional FMRP deficits and large repeat expansions into the full mutation range in a new fragile X permutation mouse model. Gene 395, 125–134.
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