TY  - GEN 
AU  - Sawamoto, K.
AU  - Gonzalez, J. V. A.
AU  - Piechnik, M.
AU  - Otero, F. J.
AU  - Couce Pico,  María Luz
AU  - Suzuki, Y.
AU  - Tomatsu, S.
PY  - 2020
SN  - 1422-0067
UR  - http://hdl.handle.net/20.500.11940/16698
AB  - Mucopolysaccharidosis type IVA (MPS IVA, or Morquio syndrome type A) is an inherited metabolic lysosomal disease caused by the deficiency of the N-acetylglucosamine-6-sulfate sulfatase enzyme. The deficiency of this enzyme accumulates the specific...
KW  - Nanomedicine
KW  - Glycosaminoglycans
KW  - Keratan Sulfate
KW  - Enzyme Replacement Therapy
KW  - Osteochondrodysplasias
KW  - Hematopoietic Stem Cell Transplantation
KW  - Quality of Life
KW  - Mucopolysaccharidosis III
KW  - Bone and Bones
KW  - Genetic Therapy
KW  - Humans
KW  - Lysosomes
KW  - Early Diagnosis
KW  - Mucopolysaccharidosis IV
KW  - Cartilage
KW  - Chondroitin Sulfates
TI  - Mucopolysaccharidosis IVA: Diagnosis, Treatment, and Management
DO  - 10.3390/ijms21041517
KW  - CHUS
KW  - IDIS
VL  - 21
ER  -