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Mucopolysaccharidosis type I Hurler-Scheie syndrome: A rare case report
Mucopolysaccharidosis I (MPS I) is a rare inherited disorder that belongs to a group of clinically progressive disorders and is caused by the deficiency of the lysosomal enzyme, α(1)-iduronidase. MPS I has been recently classified into a severe (Hurler syndrome) and an attenuated type (Hurler-Scheie...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications Pvt Ltd
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3220181/ https://ncbi.nlm.nih.gov/pubmed/22114460 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0976-237X.79287 |
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