Hereditary sensory and autonomic neuropathy II due to novel mutation in the HSN2 gene in Mexican families

被引：14
|
作者：
Pacheco-Cuellar, G. [1 ]
Gonzalez-Huerta, L. M. [1 ]
Valdes-Miranda, J. M. [1 ]
Pelaez-Gonzalez, H. [2 ]
Zenteno-Bacheron, S. [3 ]
Cazarin-Barrientos, J. [4 ]
Cuevas-Covarrubias, S. A. [1 ]
机构：
[1] Univ Nacl Autonoma Mexico, Serv Genet, Fac Med, Hosp Gen Mexico, Mexico City 06726, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Serv Radiol & Imagen, Fac Med, Hosp Gen Mexico, Mexico City 06726, DF, Mexico
[3] Univ Nacl Autonoma Mexico, Serv Neurol, Fac Med, Hosp Gen Mexico, Mexico City 06726, DF, Mexico
[4] Univ Nacl Autonoma Mexico, Serv Dermatol, Fac Med, Hosp Gen Mexico, Mexico City 06726, DF, Mexico
来源：
JOURNAL OF NEUROLOGY | 2011年 / 258卷 / 10期
关键词：
STOP CODON; PATIENT; PROTEIN; TYPE-2;
D O I：
10.1007/s00415-011-6025-x
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：1890 / 1892
页数：3
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