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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Veröffentlicht in:	Proc Natl Acad Sci U S A
Hauptverfasser:	DeLuca, Chester, Brown, Judith A., Shows, Thomas B.
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	National Academy of Sciences 1979
Schlagworte:	Biological Sciences: Genetics
Online-Zugang:	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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