Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Hyperphagia and LEPR[original query] |
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Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor. The New England journal of medicine 2007 Jan 356 (3): 237-47. Farooqi I Sadaf, Wangensteen Teresia, Collins Stephan, Kimber Wendy, Matarese Giuseppe, Keogh Julia M, Lank Emma, Bottomley Bill, Lopez-Fernandez Judith, Ferraz-Amaro Ivan, Dattani Mehul T, Ercan Oya, Myhre Anne Grethe, Retterstol Lars, Stanhope Richard, Edge Julie A, McKenzie Sheila, Lessan Nader, Ghodsi Maryam, De Rosa Veronica, Perna Francesco, Fontana Silvia, Barroso Inês, Undlien Dag E, O'Rahilly Steph |
Functional characterization of all missense variants in LEPR, PCSK1, and POMC genes arising from single-nucleotide variants. Expert review of endocrinology & metabolism 2023 3 1-11. Shah Bhavik P, Sleiman Patrick M, Mc Donald Jessica, Moeller Ida H, Kleyn Patri |
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