共 12 条
Fragile X tremor/ataxia syndrome: Blame the messenger!
被引:14
作者:

Swanson, Maurice S.
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机构: Univ Minnesota, Inst Human Genet, Minneapolis, MN 55455 USA

Orr, Harry T.
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机构: Univ Minnesota, Inst Human Genet, Minneapolis, MN 55455 USA
机构:
[1] Univ Minnesota, Inst Human Genet, Minneapolis, MN 55455 USA
[2] Univ Florida, Coll Med, Dept Mol Genet & Microbiol, Gainesville, FL 32610 USA
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D O I:
10.1016/j.neuron.2007.07.032
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
rCGG repeats in premutant alleles of the fragile X gene (FMR1) cause neurodegeneration in Drosophil and are thought to cause fragile X-associated tremor/ataxia syndrome in humans. Two reports in this issue of Neuron (Jin et al. and Sofola et al.) present data indicating a disease mechanism involving disruption of RNA-binding protein function.
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页码:535 / 537
页数:3
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共 12 条
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