A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction-Reference-Cited by-同舟云学术

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

Published:2021-06 Issue:6 Volume:108 Page:1040-1052
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Ng Bobby G.,Sosicka Paulina,Fenaille François,Harroche Annie,Vuillaumier-Barrot Sandrine,Porterfield Mindy,Xia Zhi-Jie,Wagner Shannon,Bamshad Michael J.,Vergnes-Boiteux Marie-Christine,Cholet Sophie,Dalton Stephen,Dell Anne,Dupré Thierry,Fiore Mathieu,Haslam Stuart M.,Huguenin Yohann,Kumagai Tadahiro,Kulik Michael,McGoogan Katherine,Michot Caroline,Nickerson Deborah A.,Pascreau Tiffany,Borgel Delphine,Raymond Kimiyo,Warad Deepti,Flanagan-Steet Heather,Steet Richard,Tiemeyer Michael,Seta Nathalie,Bruneel Arnaud,Freeze Hudson H.

Funder

Fondation Maladies Rares

National Institutes of Health

Commissariat à l'Energie Atomique et aux Energies Alternatives

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference45 articles.

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