Search Results - G. Matthijs
- Showing 1 - 1 results of 1
-
1
A PMM2-CDG caused by an A108V mutation associated with a heterozygous 70 kilobases deletion case report by E. Lebredonchel, A. Riquet, D. Neut, F. Broly, G. Matthijs, A. Klein, F. Foulquier
Published 2022Call Number: Loading…Connect to this object online.
Located: Loading…
Book