Codon 219 polymorphism of PRNP in healthy Caucasians and Creutzfeldt-Jakob disease patients.
作者信息
Petraroli R, Pocchiari M
出版信息
Am J Hum Genet. 1996 Apr;58(4):888-9.
Abstract
摘要
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本文引用的文献
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The original Gerstmann-Sträussler-Scheinker family of Austria: divergent clinicopathological phenotypes but constant PrP genotype.奥地利最初的格斯特曼-施特劳斯勒-谢inker家族：临床病理表型各异但朊蛋白基因型恒定。
Brain Pathol. 1995 Jul;5(3):201-11. doi: 10.1111/j.1750-3639.1995.tb00596.x.
2
Iatrogenic Creutzfeldt-Jakob disease: an example of the interplay between ancient genes and modern medicine.医源性克雅氏病：古代基因与现代医学相互作用的一个例子。
Neurology. 1994 Feb;44(2):291-3. doi: 10.1212/wnl.44.2.291.
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Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD).患有克雅氏病（CJD）的利比亚犹太人中朊蛋白基因的突变与多态性。
Am J Hum Genet. 1993 Oct;53(4):828-35.
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Prions and related neurological diseases.朊病毒与相关神经疾病
Mol Aspects Med. 1994;15(3):195-291. doi: 10.1016/0098-2997(94)90042-6.
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Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease.意大利克雅氏病患者朊蛋白基因的多态性
Hum Genet. 1994 Oct;94(4):375-9. doi: 10.1007/BF00201596.
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A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.
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New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome.患有格斯特曼-施特劳斯勒综合征的一个日本家族中的新型变异朊病毒蛋白
Brain Res Mol Brain Res. 1995 Jun;30(2):385-8. doi: 10.1016/0169-328x(95)00034-p.
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The transmissible spongiform encephalopathies.传染性海绵状脑病
Annu Rev Med. 1995;46:57-65. doi: 10.1146/annurev.med.46.1.57.
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Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome.一种朊病毒蛋白错义变体与格斯特曼-施特劳斯勒综合征的关联。
Nature. 1989 Mar 23;338(6213):342-5. doi: 10.1038/338342a0.
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Codon 129 changes in the prion protein gene in Caucasians.白种人朊蛋白基因中的密码子129变化。
Am J Hum Genet. 1990 Jun;46(6):1215-6.
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