Familial Ebstein's anomaly: whole exome sequencing identifies novel phenotype associated with FLNA

被引：0
|
作者：
Mercer, C. L. [1 ]
Andreoeltti, G. [2 ]
Carroll, A. [3 ]
Salmon, A. P. [3 ]
Temple, I. K. [2 ]
Ennis, S. [2 ]
机构：
[1] Univ Hosp Southampton NHS Fdn Trust, Wessex Clin Genet Serv, Southampton, Hants, England
[2] Univ Southampton, Fac Med, Human Genet & Genom Med, Southampton, Hants, England
[3] Univ Hosp Southampton NHS Fdn Trust, Wessex Cardiac Unit, Southampton, Hants, England
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：
P05.28D
引用
收藏
页码：270 / 271
页数：2
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