| Literature DB >> 18230891 |
Abstract
We and others have identified several single gene defects that disrupt the molecules in the leptinmelanocortin pathway causing severe obesity in humans. In this review, we consider these human monogenic obesity syndromes and discuss how far the characterisation of these patients has informed our understanding of the physiological role of leptin and the melanocortins in the regulation of human body weight and neuroendocrine function.Entities:
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Year: 2008 PMID: 18230891 DOI: 10.1159/000115333
Source DB: PubMed Journal: Front Horm Res ISSN: 0301-3073 Impact factor: 2.606