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Family study of a novel mutation of mucopolysaccharidosis t..:
Ley-Martos, Myriam
;
Guerrero, Juan M
;
Lucas-Javato, Marta
...
http://hdl.handle.net/10668/13101. , 2018
Link:
http://hdl.handle.net/10668/13101
RT Journal T1
Family study of a novel mutation of mucopolysaccharidosis type VI with a severe phenotype and good response to enzymatic replacement therapy: Case report
UL https://suche.suub.uni-bremen.de/peid=base-ftsspa:oai:www.repositoriosalud.es:10668_13101&Exemplar=1&LAN=DE A1 Ley-Martos, Myriam A1 Guerrero, Juan M A1 Lucas-Javato, Marta A1 Remón-García, Cristina A1 García-Lozano, J Raúl A1 Colón, Cristóbal A1 Crujeiras, Pablo A1 Rodrigues, Daniel A1 Paúl-Sánchez, Pedro A1 Macher, Hada C YR 2018 K1 Child K1 Preschool K1 Enzyme Replacement Therapy K1 Glycosaminoglycans K1 Homozygote K1 Humans K1 Male K1 Mucopolysaccharidosis IV K1 N-Acetylgalactosamine-4-Sulfatase K1 Phenotype K1 Polymorphism K1 Single Nucleotide K1 Recombinant Proteins K1 beta-Galactosidase JF http://hdl.handle.net/10668/13101 LK http://hdl.handle.net/10668/13101 DO http://hdl.handle.net/10668/13101 SF ELIB - SuUB Bremen
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