A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies
A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies
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DOI:
10.1016/j.jns.2007.05.034
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发表时间:
2007-12
影响因子:
4.4
通讯作者:
M. Muglia;A. Patitucci;R. Rizzi;C. Ungaro;F. Conforti;A. Gabriele;A. Magariello;R. Mazzei;L. Motti;R. Sabadini;T. Sprovieri;N. Marcello;A. Quattrone
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文献类型:
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作者:
M. Muglia;A. Patitucci;R. Rizzi;C. Ungaro;F. Conforti;A. Gabriele;A. Magariello;R. Mazzei;L. Motti;R. Sabadini;T. Sprovieri;N. Marcello;A. Quattrone