TY  - JOUR 
AU  - Guillén-Navarro, Encarna
AU  - Domingo-Jiménez, María
AU  - Alcalde-Martín, Carlos
AU  - Couce, María
AU  - Galán-Gómez, Enrique
AU  - Alonso-Luengo, Olga
AU  - Cancho Candela, Ramon
PY  - 2013
SN  - 1750-1172
UR  - https://uvadoc.uva.es/handle/10324/66034
AB  - Background: Mucopolysaccharidosis type II (MPS II) is an inherited X-linked disease associated with a deficiency in the enzyme iduronate 2-sulfatase due to iduronate 2-sulfatase gene (IDS) mutations. Recent studies in MPS II carriers did not find...
LA  - spa
PB  - BioMed Central
TI  - Clinical manifestations in female carriers of mucopolysaccharidosis type II: a spanish cross-sectional study
DO  - 10.1186/1750-1172-8-92
ER  -