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首页> Brain: A journal of neurology> Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation.

Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation.

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作者： Lenssen PP ^[1] ; Gabreels-Festen AA ; Valentijn LJ ; Jongen PJ ; van-Beersum SE ; van-Engelen BG ; van-Wensen PJ ; Bolhuis PA ; Gabreels FJ ; Mariman EC

作者单位： Institute of Neurology, University Hospital Nijmegen, The Netherlands. ^[1]

关键词 Hereditary Motor and Sensory Neuropathies genetics peripheral myelin protein-22

发布时间 2013-11-20

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准确一般字义偏差语意偏离译文作用小提交