Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion
- 期刊名称Neurology
- 作者Pareyson, D.; Scaioli, V.; Taroni, F.; Botti, S.; Lorenzetti, D.; Solari, A.; Ciano, C.; Sghirlanzoni, A.
- 卷第46卷
- 期第4期
- 印刷ISSN0028-3878
- 电子ISSN1526-632X
- 文件大小712.00KB
- 发表时间1996-04-01
- DOI10.1212/WNL.46.4.1133
- 页码1133-1137
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