Targeted disruption of the arylsulfatase B gene results in mice resembling the phenotype of mucopolysaccharidosis VI.

Mucopolysaccharidosis VI (MPS VI) is a lysosomal storage disease with autosomal recessive inheritance caused by a deficiency of the enzyme arylsulfatase B (ASB), which is involved in degradation of dermatan sulfate and chondroitin 4-sulfate. A MPS VI mouse model was generated by targeted disruption...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Evers, M, Saftig, P, Schmidt, P, Hafner, A, McLoghlin, D B, Schmahl, W, Hess, B, von Figura, K, Peters, C
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1996
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC38649/
https://ncbi.nlm.nih.gov/pubmed/8710849
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