首页> 中文期刊> 《世界核心医学期刊文摘:神经病学分册》 >德国家族性ALS:奠基者效应引发超氧化物歧化酶(SOD1)突变的R115G基因起源

德国家族性ALS:奠基者效应引发超氧化物歧化酶(SOD1)突变的R115G基因起源

         

摘要

cqvip:Mutations in the gene encoding Cu/Zn superoxide dismutase (SOD1) account for approximately 20% of patients with familial amyotrophic lateral sclerosis (FALS). In this study, sequence analysis of exons 1 5 of SOD1 in a large German cohort with FALS was performed. Among 75 affected patients, who were not obviously related probands with a positive family history, nine had missense mutations in SOD1. Four of the nine probands carry the sameR115G mutation in exon 4 of the SOD1 gene. Genotyping with markers from the SOD1 locus revealed a common haplotype and shared allelic characteristics in these patients. These findings suggest that the R115G mutation in the German population originates from a common founder.

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