A New Compound Heterozygous Mutation Of BSCL2 In A Chinese Zhuang Ethnic Family With Congenital Generalized Lipodystrophy

A New Compound Heterozygous Mutation Of BSCL2 In A Chinese Zhuang Ethnic Family With Congenital Generalized Lipodystrophy

Yuan-yuan Qin,1 Xuan Zhang,1 Li-qun Xiang,1 Qing-wen Shan,2 Shou-dong Li,3 Jie Yan,1 Fa-quan Lin1 1Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Autonomous Region, People’s Republic of China; 2Department of Pediatric...

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Bibliographic Details
Main Authors: Qin Y, Zhang X, Xiang L, Shan Q, Li S, Yan J, Lin F
Format: Article
Language:English
Published: Dove Medical Press 2019-12-01
Series:Diabetes, Metabolic Syndrome and Obesity : Targets and Therapy
Subjects:
congenital generalized lipodystrophy
pigmentation
hypertriglyceridemia
diabetes
bscl2 mutation
whole exome sequencing.
Online Access:https://www.dovepress.com/a-new-compound-heterozygous-mutation-of-bscl2-in-a-chinese-zhuang-ethn-peer-reviewed-article-DMSO

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https://www.dovepress.com/a-new-compound-heterozygous-mutation-of-bscl2-in-a-chinese-zhuang-ethn-peer-reviewed-article-DMSO

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