Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Hypogonadism 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 |
Seven novel deleterious LEPR mutations found in early-onset obesity: a ?Exon6-8 shared by subjects from Reunion Island, France, suggests a founder effect. The Journal of clinical endocrinology and metabolism 2015 Mar jc20151036. Huvenne Hélène, Le Beyec Johanne, Pépin Dominique, Alili Rohia, Pigeon Kherchiche Patricia, Jeannic Erwan, Frelut Marie-Laure, Lacorte Jean-Marc, Nicolino Marc, Viard Amélie, Laville Martine, Ledoux Séverine, Tounian Patrick, Poitou Christine, Dubern Béatrice, Clément Kari |
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