Harmatz, P.; Lampe, C.; McGill, J.J.; Parini, R.; Leao-Teles, E.; Valayannopoulos, V.; Cole, T.J.; Matousek, R.; Graham, S.; Guffon, N.; Quartel, A.
(Elsevier, 2017-09)
Mucopolysaccharidosis (MPS) VI is an autosomal recessive lysosomal storage disorder arising from deficient activity
of N-acetylgalactosamine-4-sulfatase (arylsulfatase B) and subsequent intracellular accumulation of ...
