Autor/in Kurth, Ingo Bick, David P 1 Damkier, Helle H 1 Eom, Soo Hyun 1 Haapanen, Aleksi 1 Hentschke, Moritz 1 Jacobs, Stefan 1 Kang, Gil Bu 1 Kim, Hyung-Goo 1 Laatikainen, Linda M 1 Lan, Fei 1 Meliciani, Irene 1 Ozata, Metin 1 Rosenberger, Georg 1 Rudhard, York 1 Ruusuvuori, Eva 1 Schweizer, Michaela 1 Sipilä, Sampsa T 1 Tekin, Mustafa 1 Tyynelä, Jaana 1 Wenzel, Wolfgang 1 alle zeigenListe einklappen
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
Mice with targeted Slc4a10 gene disruption have small brain ventricles and show reduced neuronal excitability. Jacobs, Stefan Ruusuvuori, Eva Sipilä, Sampsa T Haapanen, Aleksi Damkier, Helle H Kurth, Ingo Hentschke, Moritz 2008 - Forschungsinformationssystem des UKE