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Disease Info Card
Deficiency Of Arylsulfatase
Information about Deficiency Of Arylsulfatase: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Deficiency Of Arylsulfatase
Most recent studies have shown that Deficiency Of Arylsulfatase shares some biological mechanisms with argininosuccinic-aciduria, arylsulfatase-a-deficiency, deficiency-of-sulfatase, demyelination, diffuse-cerebral-sclerosis-of-schilder, dysplasia, leukodystrophy, leukodystrophy-metachromatic, lipoidosis, lysosomal-storage-diseases, metachromatic-leukodystrophy-adult-type-(disorder), mucopolysaccharidoses, mucopolysaccharidosis-vi, multiple-sulfatase-deficiency-disease, nervousness, neurodegenerative-disorders, neurological-signs-and-symptoms, pfaundler-hurler-syndrome, storage-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Deficiency Of Arylsulfatase, and have been seen in publications frequently: Cell Death, Chloride Transport, Endocytosis, Excretion, Exocytosis, Humoral Immune Response, Immune Response, Lipid Storage, Localization, Myelination, Oligodendrocyte Differentiation, Pathogenesis, Pigmentation, Secretion, Sulfation, Swimming, Transport
Quite a number of genes have been found to play important roles in Deficiency Of Arylsulfatase, such as ALAS2, ARSA, ARSB, ASNA1, CD8A, DEGS1, GALC, GLB1, MAL, MBP, MTCH1, PSAP, QPCT, RPE, SLURP1, STS, SUMF1, TIRAP. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.