Diagnosis of arylsulfatase A deficiency
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference43 articles.
1. Pseudo arylsulfatase A deficiency Biosynthesis of an abnormal arylsulfatase A
2. Deficient glycosylation of arylsulfatase A in pseudo arylsulfatase-A deficiency
3. Abnormal Sulphatase Activities in Two Human Diseases (Metachromatic Leucodystrophy and Gargoylism)
4. Synthesis and maturation of cross-reactive glycoprotein in fibroblasts deficient in arylsulfatase a activity
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Metachromatic Leukodystrophy;Lysosomal Storage Disorders;2007
2. Evolutionary origins of two tightly linked mutations in arylsulfatase-A pseudodeficiency;Human Genetics;1997-11-17
3. Metachromatic Leukodystrophy;Magnetic Resonance of Myelin, Myelination, and Myelin Disorders;1995
4. Metachromatic leukodystrophy: Multiple nonfunctional and pseudodeficiency alleles in a pedigree: Problems with diagnosis and counseling;Annals of Neurology;1993-08
5. Demyelinating and Dysmyelinating Diseases;Rivista di Neuroradiologia;1993-05
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