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Gibson, W. T., Farooqi, I. S., Moreau, M., DePaoli, A. M., Lawrence, E., O'Rahilly, S., & Trussell, R. A. (2004). Congenital Leptin Deficiency Due to Homozygosity for the Delta133G Mutation: Report of Another Case and Evaluation of Response to Four Years of Leptin Therapy. The Journal of Clinical Endocrinology & Metabolism, 89, 4821-4826.
https://doi.org/10.1210/jc.2004-0376

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