Matthew P. Wilson
Leuven, VLG 3000, Belgium
Last Updated: 09/26/2026
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Found 21 publications
Mucolipidosis II: novel variants, clinical variation and assessment of HAP1 cells as a disease model.
Journal: Human molecular genetics
Published: April 03, 2026
Genetic disorders of dolichol synthesis and utilization.
Journal: Molecular genetics and metabolism
Published: July 08, 2025
Dolichol synthesis defects: a cautionary note on the use of statins.
Journal: Molecular genetics and metabolism
Published: July 01, 2025
ATP6AP2-Related Disease Caused by Splicing Defects: Abnormal Glycosylation and the First Affected Female.
Journal: Journal of inherited metabolic disease
Published: April 08, 2025
The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene.
Journal: bioRxiv : the preprint server for biology
Published: July 01, 2024
Absence of the dolichol synthesis gene DHRSX leads to N-glycosylation defects in Lec5 and Lec9 Chinese hamster ovary cells.
Journal: The Journal of biological chemistry
Published: June 18, 2024
A pseudoautosomal glycosylation disorder prompts the revision of dolichol biosynthesis.
Journal: Cell
Published: June 13, 2024
Assessment of urinary 6-oxo-pipecolic acid as a biomarker for ALDH7A1 deficiency.
Journal: Journal of inherited metabolic disease
Published: March 20, 2024
N-glycosylation as a eukaryotic protective mechanism against protein aggregation.
Journal: Science advances
Published: January 31, 2024
A pseudoautosomal glycosylation disorder prompts the revision of dolichol biosynthesis.
Journal: Cell
Published: July 12, 2023
Beyond genetics: Deciphering the impact of missense variants in CAD deficiency.
Journal: Journal of inherited metabolic disease
Published: June 15, 2023
CAMLG-CDG: a novel congenital disorder of glycosylation linked to defective membrane trafficking.
Journal: Human molecular genetics
Published: September 13, 2021
Last Updated: 09/26/2026