Publication | Open Access

Mutational Analysis of the Pro-opiomelanocortin Gene in French Obese Children Led to the Identification of a Novel Deleterious Heterozygous Mutation Located in the α-Melanocyte Stimulating Hormone Domain

ObesityMetabolic SyndromeMutational AnalysisHealth SciencesEndocrine MechanismHuman GrowthMedicineGeneticsPhysiologyGrowth HormoneNeuroendocrinologyPediatric EndocrinologyEndocrinologyAdipokinesEndocrine ResearchPro-opiomelanocortin GeneReproductive Endocrinology