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Clinical and Mutational Features of Three Chinese Children with Congenital Generalized Lipodystrophy
Author(s) -
Xueying Su,
Ruizhu Lin,
Yonglan Huang,
Huiying Sheng,
Xiaofei Li,
Tzer Hwu Ting,
Li Liu,
Xiuzhen Li
Publication year - 2016
Publication title -
journal of clinical research in pediatric endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.566
H-Index - 35
eISSN - 1308-5735
pISSN - 1308-5727
DOI - 10.4274/jcrpe.3556
Subject(s) - medicine , lipodystrophy , exon , acanthosis nigricans , hypertriglyceridemia , mutation , diabetes mellitus , pediatrics , genetics , gene , endocrinology , insulin resistance , immunology , triglyceride , biology , human immunodeficiency virus (hiv) , cholesterol , viral load , antiretroviral therapy
To investigate the clinical and molecular features of congenital generalized lipodystrophy (CGL) in three Chinese patients with various typical manifestations.

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