Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker–Warburg syndrome
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W. Halliday | K. Buysse | D. Stemple | J. van Reeuwijk | D. Chitayat | T. Roscioli | H. van Bokhoven | Gavin J. Wright | S. Blaser | D. Lefeber | E. Kamsteeg | R. Babul‐Hirji | M. Riemersma | E. van Beusekom | Yung-Yao Lin | Gareth T. Powell | C. van den Elzen