Uncommon phenotype for a codon 178 mutation of the human PrP gene.
作者信息
Laplanche J L, Chatelain J, Thomas S, Launay J M, Gaultier C, Derouesne C
出版信息
Ann Neurol. 1992 Mar;31(3):345. doi: 10.1002/ana.410310321.
PMID:1353344
Abstract
摘要
相似文献
1
Uncommon phenotype for a codon 178 mutation of the human PrP gene.人类朊蛋白基因密码子178突变的罕见表型。
Ann Neurol. 1992 Mar;31(3):345. doi: 10.1002/ana.410310321.
2
Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutation.与密码子178天冬酰胺PRNP突变相关的家族性克雅氏病的表型特征。
Ann Neurol. 1992 Mar;31(3):282-5. doi: 10.1002/ana.410310309.
3
Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin.在欧洲血统的家族中，克雅氏病与密码子178天冬酰胺PRNP突变共分离。
Ann Neurol. 1992 Mar;31(3):274-81. doi: 10.1002/ana.410310308.
4
5
Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease.患有克雅氏病的利比亚犹太人中朊蛋白基因第200密码子的突变和第129密码子的多态性。
Philos Trans R Soc Lond B Biol Sci. 1994 Mar 29;343(1306):385-90. doi: 10.1098/rstb.1994.0033.
6
Transmission of spongiform encephalopathy from a familial Creutzfeldt-Jakob disease patient of Jewish Libyan origin carrying the PRNP codon 200 mutation.一名携带PRNP密码子200突变的利比亚犹太裔家族性克雅氏病患者的海绵状脑病传播情况。
Neurology. 1992 Jun;42(6):1249-50. doi: 10.1212/wnl.42.6.1249-a.
7
8
[Analysis of the PrP gene in a Tunisian family with Creutzfeldt-Jakob disease].[对一个患有克雅氏病的突尼斯家族中朊蛋白基因的分析]
Rev Neurol (Paris). 1991;147(12):825-7.
9
Identification of a PRNP gene mutation in Jakob's original Creutzfeldt-Jakob disease family.在雅各布最初的克雅氏病家族中鉴定出PRNP基因突变。
Lancet. 1994 Jul 9;344(8915):130-1. doi: 10.1016/s0140-6736(94)91318-8.
10
[Spongiform encephalitis].[海绵状脑病]
An R Acad Nac Med (Madr). 2001;118(3):633-52.
引用本文的文献
1
Codon 178 mutation of the human prion protein gene in a German family (Backer family): sequencing data from 72-year-old celloidin-embedded brain tissue.一个德国家族（贝克尔家族）中人朊蛋白基因的密码子178突变：来自72岁火棉胶包埋脑组织的测序数据
Acta Neuropathol. 1995;89(1):96-8. doi: 10.1007/BF00294264.
2
Prions, beta-sheets and transmissible dementias: is there still something missing?朊病毒、β-折叠与传染性痴呆：是否仍有缺失之处？
Acta Neuropathol. 1995;90(2):113-25. doi: 10.1007/BF00294309.
Zotero 插件