학술논문
A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction
Document Type
Article
Author
Ng, B.G.; Sosicka, P.; Xia, Z.-J.; Freeze, H.H.; Fenaille, F.; Cholet, S.; Harroche, A.; Vuillaumier-Barrot, S.; Dupré, T.; Seta, N.; Bruneel, A.; Porterfield, M.; Wagner, S.; Kumagai, T.; Tiemeyer, M.; Bamshad, M.J.; Nickerson, D.A.; Vergnes-Boiteux, M.-C.; Fiore, M.; Dalton, S.; Kulik, M.; Dell, A.; Haslam, S.M.; Huguenin, Y.; McGoogan, K.; Michot, C.; Pascreau, T.; Borgel, D.; Raymond, K.; Warad, D.; Flanagan-Steet, H.; Steet, R.
Source
In: American Journal of Human Genetics . (American Journal of Human Genetics, 3 June 2021, 108(6):1040-1052)
Subject
Language
English
ISSN
15376605
00029297
00029297