TY - GEN 
AU - Cabarcas L.
AU - Ramón J.L.
AU - Espinosa E.
AU - Guerrero G.D.P.
AU - Martínez N.
AU - Santamaría N.
AU - Lince I.
AU - Reyes S.
PY - 2024
SN - 2100010
UR - http://hdl.handle.net/10818/62772
AB - Introduction. Mucopolysaccharidosis type III (MPS III), also known as Sanfilippo syndrome, is a lysosomal storage disease with progressive neurodegenerative features, predominantly affecting the central nervous system. Diagnosis is based on clinical...
LA - eng
PB - Revista de Neurologia
KW - Behavioural disturbances
KW - Genetic
KW - Glycosaminoglycans
KW - Heparan sulfate
KW - Mucopolysaccharidosis
KW - Phenotype
TI - Natural history of mucopolysaccharidosis type III in a series of Colombian patients
DO - 10.33588/rn.7806.2023281
ER -