Mutations in a novel gene cause hereditary sensory and autonomic neuropathy type II.

被引:0
|
作者
Samuels, M
Lafreniere, R
MacDonald, M
MacFarlane, J
Dube, MP
O'Driscoll, M
Meilleur, S
Thompson, J
Goldberg, YP
Brais, B
Pryse-Phillips, W
Green, R
Younghusband, B
Hayden, M
Sherrington, R
Rouleau, G
机构
[1] Xenon Genet Inc, Burnaby, BC, Canada
[2] Xenon Genet Res Inc, Montreal, PQ, Canada
[3] Mem Univ Newfoundland, Fac Med, Discipline Genet, St Johns, NF, Canada
[4] Univ Montreal, Dept Med, Montreal, PQ H3C 3J7, Canada
[5] Univ British Columbia, Dept Med Genet, Vancouver, BC V5Z 1M9, Canada
[6] McGill Univ, Neurosci Res Ctr, Montreal, PQ, Canada
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
152
引用
收藏
页码:192 / 192
页数:1
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