Browsing Centre for Genomics and Child Health by Author "Wright, GJ"
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Missense mutations in-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause WalkerWarburg syndrome
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 (2013-05-01)