Whole exome sequencing reduce diagnostic odyssey of patients with epilepsy and intellectual disability

被引：0
|
作者：
Minardi, R. [1 ]
Laura, L. [1 ,2 ]
Pippucci, T. [3 ]
Baroni, M. C. [4 ]
Stipa, C. [1 ]
Mostacci, B. [1 ]
Severi, G. [3 ]
Carelli, V. [1 ,2 ]
Seri, M. [3 ]
Tinuper, P. [1 ,2 ]
Bisulli, F. [1 ,2 ]
机构：
[1] Ist Sci Neurol Bologna, IRCCS, UOC Neurol Clin, Bologna, Italy
[2] Univ Bologna, Dept Biomed & Neuromotor Sci, Bologna, Italy
[3] Polyclin St Orsola Malpighi Univ Hosp, Med Genet Unit, Bologna, Italy
[4] Univ Bologna, Dept Biomed & Surg Sci DIMEC, Bologna, Italy
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2020年 / 28卷 / SUPPL 1期
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：
P15.72.A
引用
收藏
页码：612 / 613
页数：2
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