Therapies for the bone in mucopolysaccharidoses

Patients with mucopolysaccharidoses (MPS) have accumulation of glycosaminoglycans in multiple tissues which may cause coarse facial features, mental retardation, recurrent ear and nose infections, inguinal and umbilical hernias, hepatosplenomegaly, and skeletal deformities. Clinical features related...

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Dades bibliogràfiques
Publicat a:Mol Genet Metab
Autors principals: Tomatsu, Shunji, Alméciga-Díaz, Carlos J., Montaño, Adriana M., Yabe, Hiromasa, Tanaka, Akemi, Dung, Vu Chi, Giugliani, Roberto, Kubaski, Francyne, Mason, Robert W., Yasuda, Eriko, Sawamoto, Kazuki, Mackenzie, William, Suzuki, Yasuyuki, Orii, Kenji E., Barrera, Luis A., Sly, William S., Orii, Tadao
Format: Artigo
Idioma:Inglês
Publicat: 2014
Matèries:
Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4312706/
https://ncbi.nlm.nih.gov/pubmed/25537451
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2014.12.001
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