Novel Nonsense Mutation in ASXL3 causing Bainbridge-Ropers Syndrome

被引：0
|
作者：
Lingyan Qiao
Yusheng Liu
Juan Ge
Tang Li
机构：
[1] Qingdao University,Medical Department
[2] Qingdao Women and Children’s Hospital,Department of Pediatric Endocrinology and Genetic Metabolic Diseases
[3] The Affiliated Hospital of Qingdao University,Department of Pediatric Surgery
来源：
Indian Pediatrics | 2019年 / 56卷
关键词：
Hypersomnia; Mutation; Whole-exome sequencing;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
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页码：792 / 794
页数：2
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