Screening for causative structural variants in neurological disorders using long-read sequencing

被引：0
|
作者：
Ekholm, J. [1 ]
Kujawa, S. [1 ]
Tsai, Y. [1 ]
Greenberg, D. [1 ]
Hon, T. [1 ]
Eng, K. [1 ]
Wenger, A. [1 ]
Tseng, E. [1 ]
Wang, J. [2 ]
Jarosz, M. [2 ]
Giorda, K. [2 ]
Clark, T. [1 ]
机构：
[1] Pacific Biosci, Menlo Pk, CA USA
[2] Integrated DNA Technol, Coralville, IA USA
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2018年 / 26卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P14.089A
引用
收藏
页码：671 / 672
页数：2
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