Four novel ARSA 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...
Main Authors: | Manshadi, Masoumeh Dehghan, Kamalidehghan, Behnam, Aryani, Omid, Khalili, Elham, Dadgar, Sepideh, Tondar, Mahdi, Ahmadipour, Fatemeh, Goh, Yong Meng, Houshmand, Massoud |
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Format: | Article |
Language: | English |
Published: |
Dove Medical Press
2017
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Online Access: | http://psasir.upm.edu.my/id/eprint/61916/1/Four%20novel%20ARSA%20gene%20mutations%20with%20pathogenic.pdf |
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