Four novel <em>ARSA</em> gene mutations with pathogenic impacts on metachromatic leukodystrophy: a bioinformatics approach to predict pathogenic mutations
Metachromatic leukodystrophy (MLD) disorder is a rare lysosomal storage disorder that leads to severe neurological symptoms and an early death. MLD occurs due to the deficiency of enzyme arylsulfatase A (ARSA) in leukocytes, and patients with MLD excrete sulfatide in their urine. In this study, the...
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Main Authors: | , , , , , , , , |
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Format: | Article |
Published: |
Dove Medical Press
2017
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Subjects: | |
Online Access: | http://eprints.um.edu.my/19102/ http://dx.doi.org/10.2147/TCRM.S119967 |
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Institution: | Universiti Malaya |