Schröder, Simone
Li, Yun
Yigit, Gökhan
Altmüller, Janine
Bader, Ingrid
Bevot, Andrea
Biskup, Saskia
Dreha-Kulaczewski, Steffi
Christoph Korenke, G.
Kottke, Raimund
Mayr, Johannes A.
Preisel, Martin
Toelle, Sandra P.
Wente-Schulz, Sarah
Wortmann, Saskia B.
Hahn, Heidi
Boltshauser, Eugen
Uhmann, Anja
Wollnik, Bernd
Brockmann, Knut http://orcid.org/0000-0001-6823-9091
Funding for this research was provided by:
Niedersächsisches Ministerium für Wissenschaft und Kultur (74ZN1284)
Deutsche Forschungsgemeinschaft (Research Group FOR 2800)
Germany’s Excellence Strategy (MBExC)
This article is maintained by: Elsevier
Article Title: Heterozygous truncating variants in SUFU cause congenital ocular motor apraxia
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-020-00979-w
Content Type: article
Copyright: © 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics