Genetics of Charcot-Marie-Tooth disease type 4A:: mutations, inheritance, phenotypic variability, and founder effect

被引:116
作者
Claramunt, R
Pedrola, L
Sevilla, T
de Munain, AL
Berciano, J
Cuesta, A
Sánchez-Navarro, B
Millán, JM
Saifi, GM
Lupski, JR
Vílchez, JJ
Espinós, C
Palau, F
机构
[1] CSIC, Inst Biomed, Dept Genom & Proteom, Lab Genet & Mol Med, Valencia 46010, Spain
[2] Hosp Univ La Fe, Dept Neurol, Valencia, Spain
[3] Hosp Donostia, Dept Neurol, San Sebastian, Spain
[4] Univ Cantabria, Hosp Univ Marques de Valdecilla, Dept Neurol, E-39005 Santander, Spain
[5] Hosp Univ La Fe, Genet Unit, Valencia, Spain
[6] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
关键词
D O I
10.1136/jmg.2004.022178
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
[No abstract available]
引用
收藏
页码:358 / 365
页数:8
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