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The molecular basis of Sanfilippo syndrome type B.

The Sanfilippo syndrome type B is a lysosomal storage disorder caused by deficiency of alpha-N-acetylglucosaminidase; it is characterized by profound mental deterioration in childhood and death in the second decade. For understanding the molecular genetics of the disease and for future development o...

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Autores principales: Zhao, H G, Li, H H, Bach, G, Schmidtchen, A, Neufeld, E F
Formato: Artigo
Lenguaje:Inglês
Publicado: 1996
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC39196/
https://ncbi.nlm.nih.gov/pubmed/8650226
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