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The lesions of an ovine lysosomal storage disease. Initial characterization.

An inherited disease associated with deficiencies of beta-galactosidase and alpha-neuraminidase has been identified recently in sheep. The clinical signs, the deficiency of lysosomal enzymes, and the familial nature of the disorder suggested that the condition was a lysosomal storage disease. Four a...

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Hlavní autoři: Murnane, R. D., Prieur, D. J., Ahern-Rindell, A. J., Parish, S. M., Collier, L. L.
Médium: Artigo
Jazyk:Inglês
Vydáno: 1989
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1879591/
https://ncbi.nlm.nih.gov/pubmed/2916646
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