Clinical and Molecular Genetic Spectrum of Congenital Deficiency of the Leptin Receptor

I. Sadaf Farooqi, Teresia Wangensteen, Stephan C. Collins, Wendy L. Kimber, Giuseppe Matarese, Julia M. Keogh, Emma Lank, Bill Bottomley, Judith López‐Fernández, Iván Ferraz‐Amaro, Mehul Dattani, Oya Ercan, Anne Grethe Myhre, Lars Retterstøl, R Stanhope, Julie Edge, S A McKenzie, Nader Lessan, Maryam Ghodsi, Veronica De Rosa, Francesco Perna, Silvia Fontana, Inês Barroso, Dag E. Undlien, Stephen O’Rahilly

New England Journal of Medicine, 2007

Addenbrooke's Hospital, University of Cambridge, Oslo University Hospital, University of Oslo, Wellcome Sanger Institute, Institute for Experimental Endocrinology and Oncology, University of Naples Federico II, Hospital Universitario de Canarias, Institute of Child Health, Istanbul University, Istanbul University-Cerrahpaşa, Great Ormond Street Hospital, University College London, John Radcliffe Hospital, Royal London Hospital, Shariati Hospital, Tehran University of Medical Sciences

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Abstract

This research paper explore the methodology and findings associated with New England Journal of Medicine. The study delves into the core aspects of the research field, providing significant data and citation impact. (Full abstract processing is available via the OpenAlex API).

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Clinical and Molecular Genetic Spectrum of Congenital Deficiency of the Leptin Receptor

Abstract

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