Matthew P Wilson

6PUBLICATIONS
15CO-AUTHORS
Medical biochemistry - inorganic elements and compoundsMolecular targetsMolecular medicineGene and molecular therapyEpigenetics (incl. genome methylation and epigenomics)
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Publications (6)

|Aug 10, 2026
Mucolipidosis II: novel variants, clinical variation and assessment of HAP1 cells as a disease model.

|Jul 01, 2024
The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene.

Takfarinas Kentache, Charlotte R Althoff, Francesco Caligiore

|Aug 04, 2023
Beyond genetics: Deciphering the impact of missense variants in CAD deficiency.

Francisco Del Caño-Ochoa, Bobby G Ng, Antonio Rubio-Del-Campo

|Mar 09, 2022
CAMLG-CDG: a novel congenital disorder of glycosylation linked to defective membrane trafficking.

Matthew P Wilson, Zoé Durin, Özlem Unal

|Mar 17, 2021
SLC37A4-CDG: Second patient.

Matthew P Wilson, Dulce Quelhas, Elisa Leão-Teles

|Aug 08, 2017
An LC-MS/MS-Based Method for the Quantification of Pyridox(am)ine 5'-Phosphate Oxidase Activity in Dried Blood Spots from Patients with Epilepsy.

Matthew P Wilson, Emma J Footitt, Apostolos Papandreou

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Frequent Collaborators

1 joint publications

Kevin A Mills

1 joint publications

Francisco Del Caño-Ochoa

1 joint publications

Bobby G Ng

1 joint publications

Antonio Rubio-Del-Campo