Monoallelic intragenic POU3F2 variants lead to neurodevelopmental delay and hyperphagic obesity, confirming the gene’s candidacy in 6q16.1 deletions
Titel:
Monoallelic intragenic POU3F2 variants lead to neurodevelopmental delay and hyperphagic obesity, confirming the gene’s candidacy in 6q16.1 deletions
Auteur:
Schönauer, Ria Jin, Wenjun Findeisen, Christin Valenzuela, Irene Devlin, Laura Alice Murrell, Jill Bedoukian, Emma C. Pöschla, Linda Hantmann, Elena Riedhammer, Korbinian M. Hoefele, Julia Platzer, Konrad Biemann, Ronald Campeau, Philipp M. Münch, Johannes Heyne, Henrike Hoffmann, Anne Ghosh, Adhideb Sun, Wenfei Dong, Hua Noé, Falko Wolfrum, Christian Woods, Emily Parker, Michael J. Neatu, Ruxandra Le Guyader, Gwenael Bruel, Ange-Line Perrin, Laurence Spiewak, Helena Missotte, Isabelle Fourgeaud, Melanie Michaud, Vincent Lacombe, Didier Paolucci, Sarah A. Buchan, Jillian G. Glissmeyer, Margaret Popp, Bernt Blüher, Matthias Sayer, John A. Halbritter, Jan