The gene for Huntington's disease.
作者信息
Harding A E
出版信息
BMJ. 1993 Aug 14;307(6901):396-7. doi: 10.1136/bmj.307.6901.396.
Abstract
摘要
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Ethical and social issues in presymptomatic testing for Huntington's disease: a European Community collaborative study. European Community Huntington's Disease Collaborative Study Group.亨廷顿舞蹈症症状前检测中的伦理和社会问题：一项欧洲共同体合作研究。欧洲共同体亨廷顿舞蹈症合作研究小组
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Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.1型脊髓小脑共济失调中不稳定的三核苷酸CAG重复序列的扩增。
Nat Genet. 1993 Jul;4(3):221-6. doi: 10.1038/ng0793-221.
2
Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease.用于导致亨廷顿舞蹈症的（CAG）n重复序列的改良聚合酶链式反应条件。
Hum Mol Genet. 1993 Jun;2(6):637. doi: 10.1093/hmg/2.6.637.
3
A PCR method for accurate assessment of trinucleotide repeat expansion in Huntington disease.一种用于准确评估亨廷顿舞蹈病中三核苷酸重复序列扩增的聚合酶链反应方法。
Hum Mol Genet. 1993 Jun;2(6):635-6. doi: 10.1093/hmg/2.6.635.
4
A simple non-radioactive method for diagnosis of Huntington's disease.
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Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms.人类大脑中含新型三联体重复序列的基因：克隆、表达及长度多态性
Genomics. 1993 Jun;16(3):572-9. doi: 10.1006/geno.1993.1232.
6
A polymorphic DNA marker genetically linked to Huntington's disease.一种与亨廷顿舞蹈症基因连锁的多态性DNA标记。
Nature. 1983;306(5940):234-8. doi: 10.1038/306234a0.
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Recombination events suggest potential sites for the Huntington's disease gene.重组事件提示了亨廷顿舞蹈症基因的潜在位点。
Neuron. 1989 Aug;3(2):183-90. doi: 10.1016/0896-6273(89)90031-7.
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Instability versus predictability: the molecular diagnosis of myotonic dystrophy.不稳定性与可预测性：强直性肌营养不良的分子诊断
J Med Genet. 1992 Nov;29(11):761-5. doi: 10.1136/jmg.29.11.761.
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