Deletion in prion protein gene in a Moroccan family.
作者信息
Laplanche J L, Chatelain J, Launay J M, Gazengel C, Vidaud M
机构信息
F.R.A.C. Bernard 'Neurochimie des Communications Cellulaires', Service de Biochimie, Hôpital Saint-Louis, France.
出版信息
Nucleic Acids Res. 1990 Nov 25;18(22):6745. doi: 10.1093/nar/18.22.6745.
Abstract
摘要
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本文引用的文献
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High incidence of Creutzfeldt-Jakob disease in North African immigrants to France.法国的北非移民中克雅氏病的高发病率。
Neurology. 1985 Jun;35(6):894-5. doi: 10.1212/wnl.35.6.894.
2
Molecular cloning of a human prion protein cDNA.人朊病毒蛋白cDNA的分子克隆
DNA. 1986 Aug;5(4):315-24. doi: 10.1089/dna.1986.5.315.
3
Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome.朊病毒蛋白第102位的脯氨酸-亮氨酸改变是与格斯特曼-施特劳斯勒综合征相关的最常见但并非唯一的突变。
Biochem Biophys Res Commun. 1989 Sep 15;163(2):974-9. doi: 10.1016/0006-291x(89)92317-6.
4
Diagnosis of Gerstmann-Sträussler syndrome in familial dementia with prion protein gene analysis.通过朊蛋白基因分析对家族性痴呆中的格斯特曼-施特劳斯勒综合征进行诊断。
Lancet. 1989 Jul 1;2(8653):15-7. doi: 10.1016/s0140-6736(89)90256-0.
5
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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