Lampe, C.; McNelly, B.; Gevorkian, A.K.; Hendriksz, Christian J.; Lobzhanidze, T.V.; Perez-López, J.; Stepien, K.M.; Vashakmadze, N.D.; Del Toro, M.
(Elsevier, 2019-12)
Mucopolysaccharidoses (MPS) are rare disorders associated with enzyme deficiencies, resulting in glycosaminoglycan
(GAG) accumulation in multiple organ systems. As patients increasingly survive to adulthood, the need
for ...