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Journal of Endocrinology, ISSN 0022-0795, 2016, Volume 230, Issue 1, pp. 13 - 26
Journal Article
Journal Article
MEDIZINISCHE GENETIK, ISSN 1863-5490, 12/2017, Volume 29, Issue 4, pp. 348 - 359
Autosomal recessive inherited mutations in the genes for leptin, leptin receptor, proopiomelanocortin (POMC) and prohormon convertase 1 (PC1) cause severe... 
CONGENITAL LEPTIN DEFICIENCY | ACCESSORY PROTEIN-2 | Melanocortin-4 receptor | NEUROTROPHIC FACTOR | MELANOCORTIN-4 RECEPTOR GENE | EARLY-ONSET OBESITY | DEVELOPMENTAL DELAY | POMC | BODY-WEIGHT | RECOMBINANT LEPTIN | Leptin receptor | Leptin | PROOPIOMELANOCORTIN DEFICIENCY | GENETICS & HEREDITY | HYPOGONADOTROPIC HYPOGONADISM | Monogenic obesity
Journal Article
Journal Article
ACS Biomaterials Science & Engineering, ISSN 2373-9878, 04/2018, Volume 4, Issue 4, pp. 1241 - 1250
Journal Article
Journal Article