Mutations in NSUN2 cause autosomal- Recessive intellectual disability
- Lia Abbasi-Moheb
- , Sara Mertel
- , Melanie Gonsior
- , Leyla Nouri-Vahid
- , Kimia Kahrizi
- , Sebahattin Cirak
- , Dagmar Wieczorek
- , M. Mahdi Motazacker
- , Sahar Esmaeeli-Nieh
- , Kirsten Cremer
- , Robert Weißmann
- , Andreas Tzschach
- , Masoud Garshasbi
- , Seyedeh S. Abedini
- , Hossein Najmabadi
- , H. Hilger Ropers
- , Stephan J. Sigrist
- , Andreas W. Kuss*
*Corresponding author for this work
- Max Planck Institute for Molecular Genetics
- University of Social Welfare and Rehabilitation Sciences
- Free University of Berlin
- University College London
- University of Duisburg-Essen
- University of California at San Francisco
- University of Greifswald
- University of Tübingen
- Tarbiat Modarres University
- Charité – Universitätsmedizin Berlin
Research output: Contribution to journal › Article › Academic › peer-review