Wilson, M. P. Et Al. 2022. CAMLG-CDG: a novel congenital disorder of glycosylation linked to defective membrane trafficking.. Human molecular genetics , vol.31 , 2571-2581.

Wilson, M. P., Durin, Z., Unal, Ö., Ng, B. G., Marrecau, T., Keldermans, L., ... Souche, E.(2022). CAMLG-CDG: a novel congenital disorder of glycosylation linked to defective membrane trafficking.. Human molecular genetics , vol.31, 2571-2581.

Wilson, Matthew Et Al. "CAMLG-CDG: a novel congenital disorder of glycosylation linked to defective membrane trafficking.," Human molecular genetics , vol.31, 2571-2581, 2022

Wilson, Matthew P. Et Al. "CAMLG-CDG: a novel congenital disorder of glycosylation linked to defective membrane trafficking.." Human molecular genetics , vol.31, pp.2571-2581, 2022

Wilson, M. P. Et Al. (2022) . "CAMLG-CDG: a novel congenital disorder of glycosylation linked to defective membrane trafficking.." Human molecular genetics , vol.31, pp.2571-2581.

@article{article, author={Matthew P Wilson Et Al. }, title={CAMLG-CDG: a novel congenital disorder of glycosylation linked to defective membrane trafficking.}, journal={Human molecular genetics}, year=2022, pages={2571-2581} }