Missense mutations in-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause WalkerWarburg syndrome

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Volume
22
Pagination
1746 - 1754
DOI
10.1093/hmg/ddt021
Journal
HUMAN MOLECULAR GENETICS
Issue
9
ISSN
0964-6906
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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
URI
http://qmro.qmul.ac.uk/xmlui/handle/123456789/13509
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© 2013 The Author