Author:
Carvajal Jaime J.,Pook Mark A.,Santos Maria dos,Doudney Kit,Hillermann Renate,Minogue Shane,Williamson Robert,Hsuan J. Justin,Chamberlain Susan
Publisher
Springer Science and Business Media LLC
Reference20 articles.
1. Chamberlain, S. et al. Mapping of mutation causing Friedreich's ataxia to human chromosome 9. Nature 334, 248–249 (1988).
2. Rodius, F. et al. Recombinations in individuals homozygous by descent, localize the Friedreich ataxia locus in a cloned 450-kb interval. Am. J. Hum. Genet. 54, 1050–1059 (1994).
3. Duclos, F., Rodius, F., Wrogemann, K., Mandel, J.L. & Koenig, M., Friedreich ataxia region: characterization of two novel genes and reduction of the critical region to 300kb. Hum. Molec. Genet. 3, 909–914 (1994).
4. Montermini, L. et al. The Friedreich ataxia region spans a 150-kb interval on chromosome9q13. Am. J. Hum. Genet. 57, 1061–1067 (1995).
5. Campuzano, V. et al. Friedreich's ataxia: Autosomal recessive disease caused by an intronic GAA repeat expansion. Science 271, 1423–1427 (1996).
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