Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker–Warburg syndrome
- Resource Type
- Authors
- Buysse, K.; Riemersma, M.; Powell, G.; van Reeuwijk, J.; Chitayat, D.; Roscioli, T.; Kamsteeg, E.-J.; van den Elzen, C.; van Beusekom, E.; Blaser, S.; Babul-Hirji, R.; Halliday, W.; Wright, G. J.; Stemple, D. L.; Lin, Y.-Y.; Lefeber, D. J.; van Bokhoven, H.
- Source
- Human Molecular Genetics; Vol 22
- Subject
- Language
- English
- ISSN
- 1460-2083