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Natural History and Molecular Characteristics of Korean Patients with Mucopolysaccharidosis Type III

Background: Mucopolysaccharidosis type III (MPS III) is an autosomal recessive lysosomal storage disorder characterised by progressive neurocognitive deterioration. MPS III subtypes are clinically indistinguishable, with a wide range of symptoms and variable severity. The natural history of this dis...

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Detalles Bibliográficos
Autores principales:	Kim, Min-Sun, Yang, Aram, Noh, Eu-seon, Kim, Chiwoo, Bae, Ga Young, Lim, Han Hyuk, Park, Hyung-Doo, Cho, Sung Yoon, Jin, Dong-Kyu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9145712/ https://www.ncbi.nlm.nih.gov/pubmed/35629088 http://dx.doi.org/10.3390/jpm12050665

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