Trofimova, N.S.; Olkhovich, N.V.
(Вiopolymers and Cell, 2016)
Mucopolysaccharidosis I (MPS I) is a rare hereditary autosomal-recessive metabolic disorder, which occurs due to the deficiency of the lysosomal enzyme α-L-iduronidase (IDUA; EC 3.2.1.76). There are three clinical forms ...