ESPEYB15 7 PUBERTY New genes in hypogonadotropic hypogonadism (2 abstracts)
7.10 DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development
Bouilly J , Messina A , Papadakis G , Cassatella D , Xu C , Acierno JS , Tata B , Sykiotis G , Santini S , Sidis Y , Elowe-Gruau E , Phan-Hug F , Hauschild M , Bouloux PM , Quinton R , Lang-Muritano M , Favre L , Marino L , Giacobini P , Dwyer AA , Niederländer NJ & Pitteloud N
Endocrinology, Diabetes & Metabolism Service, Centre Hospitalier Universitaire Vaudois (CHUV), Faculty of Biology & Medicine, University of Lausanne, Lausanne, Switzerland
To read the full abstract: Hum Mol Genet. 2018 Jan 15;27(2):359-372
Volume 15
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ESPE Yearbook of Paediatric Endocrinology
ISSN 1662-4009 (Online)
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