Identification of 17 novel mutations in 40 Argentinean unrelated families with mucopolysaccharidosis type II (Hunter syndrome)

Mucopolysaccharidosis type II (MPSII) is an X-linked lysosomal storage disorder caused by deficiency of the enzyme iduronate-2-sulfatase (IDS). The human IDS gene is located in chromosome Xq28. This is the first report of genotype and phenotype characterization of 49 Hunter patients from 40 families...

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Detalles Bibliográficos
Autores principales: Amartino, H., Ceci, R., Masllorens, F., Gal, A., Arberas, C., Bay, L., Ilari, R., Dipierri, J., Specola, N., Cabrera, A., Rozenfeld, P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121352/
https://www.ncbi.nlm.nih.gov/pubmed/27896113
http://dx.doi.org/10.1016/j.ymgmr.2014.08.006

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121352/
https://www.ncbi.nlm.nih.gov/pubmed/27896113
http://dx.doi.org/10.1016/j.ymgmr.2014.08.006

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