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October 1, 2004The Journal of Clinical Endocrinology & MetabolismOpen Access

Congenital Leptin Deficiency Due to Homozygosity for the Δ133G Mutation: Report of Another Case and Evaluation of Response to Four Years of Leptin Therapy

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Authors

WGWilliam T. GibsonBritish Columbia Children's Hospital
I. Sadaf Farooqi
I. Sadaf FarooqiInternational University of SarajevoMMMary MoreauAlberta Children's Hospital

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Gibson et al. (2004) studied this question.

synapsesocial.com/papers/6a6f53c4f44fa9f079dcc054https://doi.org/10.1210/jc.2004-0376
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