Analysis of a Chinese pedigree with Zellweger syndrome reveals a novel PEX1 mutation by next-generation sequencing
Authors:
- Lixia WangLWLixia Wang
- Xiaoming WeiXWXiaoming Wei
- Qian ZhuQZQian Zhu
- Yun YangYYYun Yang
- Zhangzhang LanZLZhangzhang Lan
- Ning QuNQNing Qu
- Yuxing ChuYCYuxing Chu
- Yuhui WangYWYuhui Wang
- Shuang YangSYShuang Yang
- Yu LiangYLYu Liang
- Wei WangWWWei Wang
- 1 February 2013
- journal article
- case report
- Published by Elsevier in Clinica Chimica Acta
- Vol. 417, 57-61
Abstract
No abstract availableKeywords
Funding Information
- Development and Reform Commission of Shenzhen Municipality
- Guangdong Provincial Department of Science and Technology
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