A novel 3'-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies.

导出原文传递

翻译打印收藏纠错

作者： Meuleman J ^[1] ; Pou-Serradell A ^[2] ; Lofgren A ; Ceuterick C ; Martin JJ ; Timmerman V ; Van-Broeckhoven C ; De-Jonghe P

作者单位： Department of Molecular Genetics, Flanders Interuniversity Institute for Biotechnology, University of Antwerp, Antwerpen, Belgium. ^[1] artners.org ^[2]

关键词 DNA Recombinant Hereditary Motor and Sensory Neuropathies genetics Mutation 重组突变髓磷脂蛋白质类麻痹

发布时间 2013-11-20

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交

浏览0

Neuromuscular disorders

2001年11卷4期

400-403页

相似文献

中文期刊
外文期刊
学位论文
会议论文

检索历史清除

A novel 3'-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies.

Neuromuscular disorders

相似文献

Neuromuscular disorders

相关期刊

参考文献：
指定格式：	NoteExpress EndNote RefWorks NoteFirst

检索历史 清除

A novel 3'-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies.

Neuromuscular disorders

相似文献

Neuromuscular disorders

相关期刊

检索历史清除