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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Detaylı Bibliyografya
Asıl Yazarlar: DeLuca, Chester, Brown, Judith A., Shows, Thomas B.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1979
Konular:
Biological Sciences: Genetics
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC383512/
https://ncbi.nlm.nih.gov/pubmed/36611
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