About: A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction   Goto Sponge  NotDistinct  Permalink

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  • Ng Bobby, Sosicka Paulina, Fenaille François, Harroche Annie, Vuillaumier-Barrot Sandrine, Porterfield Mindy, Xia Zhi-Jie, Wagner Shannon, Bamshad Michael, Vergnes-Boiteux Marie-Christine, Cholet Sophie, Dalton Stephen, Dell Anne, Dupré Thierry, Fiore Mathieu, Haslam Stuart, Huguenin Yohann, Kumagai Tadahiro, Kulik Michael, McGoogan Katherine, Michot Caroline, Nickerson Deborah, Pascreau Tiffany, Borgel Delphine, Raymond Kimiyo, Warad Deepti, Flanagan-Steet Heather, Steet Richard, Tiemeyer Michael, Seta Nathalie, Bruneel Arnaud. A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction. American Journal of Human Genetics, Elsevier (Cell Press), 2021, 108 (6), pp.1040-1052. ⟨10.1016/j.ajhg.2021.04.013⟩
Title
  • A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction
dc:date
  • 2021
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