Whole exome sequencing in patients with congenital myopathies

被引：2
|
作者：
Zaharieva, I. T. [1 ]
Colombo, I. [2 ]
Sframeli, M. [1 ]
Sigurosson, J. H. [3 ]
Feng, L. [1 ]
Phadke, R. [1 ]
Sewry, C. A. [1 ]
Morgan, J. E. [1 ]
Muntoni, F. [1 ]
机构：
[1] UCL, London, England
[2] Univ Milan, Milan, Italy
[3] DeCODE Genet, Reykjavik, Iceland
来源：
NEUROMUSCULAR DISORDERS | 2014年 / 24卷 / 9-10期
关键词：
D O I：
10.1016/j.nmd.2014.06.337
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
G.P.261
引用
收藏
页码：895 / 895
页数：1
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