Autor/in Popp, Bernt Airik, Rannar 1 Amann, Kerstin 1 Endele, Sabine 1 Fritsch, Angela 1 Geider, Kirsten 1 Hellenbroich, Yorck 1 Knaup, Karl X 1 Kortüm, Fanny 1 Milh, Mathieu 1 Pientka, Friederike K 1 Reis, André 1 Rosenberger, Georg 1 Schiffer, Mario 1 Schwarz, Hannah 1 Stefanova, Irina 1 Stoeckert, Johanna 1 Tamer, Ceyhun 1 Torabi, Nasrin 1 Wiech, Thorsten 1 Wiesener, Michael S 1 alle zeigenListe einklappen
Biallelic ANKS6 mutations cause late-onset ciliopathy with chronic kidney disease through YAP dysregulation Schwarz, Hannah Popp, Bernt Airik, Rannar Torabi, Nasrin Knaup, Karl X Stoeckert, Johanna Wiech, Thorsten 2022 - Forschungsinformationssystem des UKE
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes. Endele, Sabine Rosenberger, Georg Geider, Kirsten Popp, Bernt Tamer, Ceyhun Stefanova, Irina Milh, Mathieu 2010 - Forschungsinformationssystem des UKE
