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A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction |
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Titel: |
A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction |
Auteur: |
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. |
Verschenen in: |
The American journal of human genetics |
Paginering: |
Jaargang 108 () nr. 6 pagina's 1040-1052 |
Jaar: |
2021 |
Inhoud: |
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Uitgever: |
American Society of Human Genetics |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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