Accurately resolving copy number variation in highly homologous SMN1 and SMN2 genes using next-generation sequencing and rhPCR

被引：0
|
作者：
Junnila, H. [1 ]
Valori, M. [1 ]
Korppoo, A. [1 ]
Koskinen, L. [1 ]
Salminen, E. [1 ]
Gall, K. [1 ]
Alastalo, T. [1 ]
Myllykangas, S. [1 ]
Koskenvuo, J. [1 ]
Salmenpera, P. [1 ]
Sistonen, J. [1 ]
机构：
[1] Blueprint Genet, Helsinki, Finland
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2019年 / 27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：
P10.34A
引用
收藏
页码：1488 / 1488
页数：1
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