A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction

A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction

B. G. Ng, P. Sosicka, F. Fenaille, A. Harroche, S. Vuillaumier-Barrot, M. Porterfield, Z. J. Xia, S. Wagner, M. J. Bamshad, M. C. Vergnes-Boiteux, S. Cholet, S. Dalton, A. Dell, T. Dupre, M. Fiore, S. M. Haslam, Y. Huguenin, T. Kumagai, M. Kulik, K. McGoogan, C. Michot, D. A. Nickerson, T. Pascreau, D. Borgel, K. Raymond, D. Warad, G. University of Washington Center for Mendelian, H. Flanagan-Steet, R. Steet, M. Tiemeyer, N. Seta, A. Bruneel and H. H. Freeze