B. G. Ng

Neurology of inherited glycosylation disorders

H. Freeze, E. Eklund, B. G. Ng, 2012, The Lancet Neurology.

Congenital Disorders of Glycosylation

H. Freeze, B. G. Ng, P. Sosicka, 2021, Comprehensive Glycoscience.

Human genetic disorders involving glycosylphosphatidylinositol (GPI) anchors and glycosphingolipids (GSL)

H. Freeze, B. G. Ng, B. Ng, 2015, Journal of Inherited Metabolic Disease.

Predominant and novel de novo variants in 29 individuals with ALG13 deficiency: Clinical description, biomarker status, biochemical analysis, and treatment suggestions

Undiagnosed Diseases Network, J. Rosenfeld, I. Scheffer, 2020, Journal of inherited metabolic disease.

Dissecting Functions of the Conserved Oligomeric Golgi Tethering Complex Using a Cell-Free Assay

H. Freeze, B. G. Ng, D. Ungar, 2013, Traffic.

COG8 deficiency causes new congenital disorder of glycosylation type IIh.

H. Freeze, E. Eklund, B. G. Ng, 2007, Human molecular genetics.

Glycomics, Glycobiology, and Glyco-Medicine

H. Freeze, B. G. Ng, B. Ng, 2013 .

Molecular and clinical characterization of a Moroccan Cog7 deficient patient.

H. Freeze, B. G. Ng, M. Durán, 2007, Molecular genetics and metabolism.