A Novel Heterozygous Mutation in Peroxisome Proliferator-Activated Receptor-γ Gene in a Patient with Familial Partial Lipodystrophy-Reference-Cited by-同舟云学术

A Novel Heterozygous Mutation in Peroxisome Proliferator-Activated Receptor-γ Gene in a Patient with Familial Partial Lipodystrophy

Published:2002-01-01 Issue:1 Volume:87 Page:408-408
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Agarwal Anil K.¹,Garg Abhimanyu¹

Affiliation:

1. Department of Internal Medicine, Division of Nutrition and Metabolic Diseases and Center for Human Nutrition, University of Texas Southwestern Medical Center, Dallas, Texas 75390

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/87/1/408/9159155/jcem0408.pdf

Cited by 20 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. CANDLE-ПОДОБНЫЙ СИНДРОМ: КЛИНИЧЕСКОЕ НАБЛЮДЕНИЕ;Azerbaijan Medical Journal;2023-12-20

2. Case Report: A New Peroxisome Proliferator-Activated Receptor Gamma Mutation Causes Familial Partial Lipodystrophy Type 3 in a Chinese Patient;Frontiers in Endocrinology;2022-03-29

3. Developmental origins of metabolic diseases;Physiological Reviews;2021-07-01

4. Case Report: Metreleptin Treatment in a Patient With a Novel Mutation for Familial Partial Lipodystrophy Type 3, Presenting With Uncontrolled Diabetes and Insulin Resistance;Frontiers in Endocrinology;2021-06-08

5. From Food to Genes: Transcriptional Regulation of Metabolism by Lipids and Carbohydrates;Nutrients;2021-04-30