Uncovering the molecular mechanisms behind disease-associated leptin variants
Author:
Funder
National Science Foundation (NSF)
Welch Foundation
National Institute of General Medical Sciences
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference70 articles.
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3. Human Leptin Deficiency Caused by a Missense Mutation: Multiple Endocrine Defects, Decreased Sympathetic Tone, and Immune System Dysfunction Indicate New Targets for Leptin Action, Greater Central than Peripheral Resistance to the Effects of Leptin, and Spontaneous Correction of Leptin-Mediated Defects
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