Lysosomal arylsulfatase deficiencies in humans: Chromosome assignments for arylsulfatase A and B
Genetics of human lysosomal arylsulfatases A and B (aryl-sulfate sulfohydrolase, EC 3.1.6.1), associated with childhood disease, has been studied with human-rodent somatic cell hybrids. Deficiency of arylsulfatase A (ARS(A)) in humans results in a progressive neurodegenerative disease, metachromatic...
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| Vydáno v: | Proc Natl Acad Sci U S A |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
1979
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC383512/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/36611/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.76.4.1957 |
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