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

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

DOI Full Paper Access

19

Citations

36

References

2021

Year

Bobby Ng, Paulina Sosicka, François Fenaille, Annie Harroche, Sandrine Vuillaumier‐Barrot, Mindy Porterfield, Zhi‐Jie Xia, Shannon M. Wagner, Michael J. Bamshad, Marie-Christine Vergnes-Boiteux,

The American Journal of Human Genetics

Somatic VariantMendelian DisorderGenetic DisorderLiver PhysiologyInherited Metabolic DiseaseGlycobiologyGeneticsMolecular BiologyPathologyLiver DysfunctionCongenital DisorderMolecular GeneticsDisease Gene IdentificationMedicineLysosomal Storage Disease

References

	Year	Citations

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