NOVEL MUTATION DETECTED BY WHOLE EXOME SEQUENCING IN A PATIENT WITH SATB2-ASSOCIATED SYNDROME

被引：0
|
作者：
Nasomyont, N. [1 ]
Martinez, J. [1 ]
机构：
[1] Univ S Alabama, Mobile, AL USA
来源：
JOURNAL OF INVESTIGATIVE MEDICINE | 2017年 / 65卷 / 02期
关键词：
D O I：
10.1136/jim-2016-000393.323
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
323
引用
收藏
页码：524 / 525
页数：2
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