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Clinical and Molecular Genetic Spectrum of Congenital Deficiency of the Leptin ReceptorDOI 10.1016/s0084-3954(08)70507-4
Monogenic forms of childhood obesity due to mutations in the leptin geneSemantic proximity
Congenital leptin deficiency is associated with severe early-onset obesity in humansSemantic proximity
Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor.Semantic proximity
Congenital leptin and leptin receptor deficiencies in nine new families: identification of six novel variants and review of literature.Semantic proximity
When Leptin Is Not There: A Review of What Nonsyndromic Monogenic Obesity Cases Tell Us and the Benefits of Exogenous Leptin.Semantic proximity
A National Multicenter Study of Leptin and Leptin Receptor Deficiency and Systematic Review.Semantic proximity
The involvement of leptin in humans revealed by mutations in leptin and leptin receptor genes.Semantic proximity
Leptin: molecular biology, physiology, and relevance to pediatric practice.Semantic proximity
High morbidity and mortality in children with untreated congenital deficiency of leptin or its receptorSemantic proximity
Exon skipping and severe childhood-onset obesity caused by a leptin receptor mutation.Semantic proximity
Functional and Phenotypic Characteristics of Human Leptin Receptor MutationsSemantic proximity
Leptin Receptor Compound Heterozygosity in Humans and Animal Models.Semantic proximity
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