Penco S, Schenone A, Bordo D, Bolognesi M, Abbruzzese M, Bugiani O, Ajmar F, Garrè C
Department of Oncology, University of Genova, Italy.
Neurology. 1999 Jul 22;53(2):404-6. doi: 10.1212/wnl.53.2.404.
We report a new missense mutation (Gly12Arg) [corrected] in exon 1 of the Cu/Zn superoxide dismutase (SOD1) gene in a 67-year-old patient with familial ALS (FALS). The clinical course showed an unusually slow progression. The enzymatic activity of the mutated SOD1 was 80% of normal. At the molecular level, the Gly12Arg [corrected] mutation occurs in a region outside the active site and may lead to local distortion strain in the protein structure.
我们报告了一名67岁家族性肌萎缩侧索硬化症(FALS)患者铜/锌超氧化物歧化酶(SOD1)基因外显子1中的一个新错义突变(Gly12Arg)[已校正]。临床病程显示进展异常缓慢。突变型SOD1的酶活性为正常活性的80%。在分子水平上,Gly12Arg[已校正]突变发生在活性位点之外的区域,可能导致蛋白质结构中的局部扭曲应变。