Autor/in Kim, Hyung-Goo 2 Kurth, Ingo 2 Meliciani, Irene Wenzel, Wolfgang 2 Ahn, Jang-Won 1 Bick, David P 1 Eom, Soo Hyun 1 Ha, Kyung-Soo 1 Itokawa, Yasuhide 1 Kang, Gil Bu 1 Kim, Hyun-Taek 1 Kulharya, Anita 1 Lan, Fei 1 Lee, Deresa 1 Ozata, Metin 1 Rosenberger, Georg 1 Tekin, Mustafa 1 Ullmann, Reinhard 1 alle zeigenListe einklappen
WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. Kim, Hyung-Goo Ahn, Jang-Won Kurth, Ingo Ullmann, Reinhard Kim, Hyun-Taek Kulharya, Anita Ha, Kyung-Soo 2010 - Forschungsinformationssystem des UKE
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. Kim, Hyung-Goo Kurth, Ingo Lan, Fei Meliciani, Irene Wenzel, Wolfgang Eom, Soo Hyun Kang, Gil Bu 2008 - Forschungsinformationssystem des UKE
