Journal article
Identification of nine novel arylsulfatase a (ARSA) gene mutations in patients with metachromatic leukodystrophy (MLD)
Abstract
Metachromatic leukodystrophy (MLD) is a rare autosomal recessive disorder caused by mutations of the arylsulfatase A (ARSA) gene. We have investigated more than fifty MLD patients using allele-specific PCR assays to detect the pseudodeficiency (PD) allele and several common MLD mutations, followed by comprehensive nucleotide sequencing of the ARSA gene to detect rare or private mutations. Here we report the identification of nine novel …
Authors
Eng B; Nakamura LN; O'Reilly N; Schokman N; Nowaczyk MMJ; Krivit W; Waye JS
Journal
Human Mutation, Vol. 22, No. 5, pp. 418–419
Publisher
Hindawi
Publication Date
November 2003
DOI
10.1002/humu.9190
ISSN
1059-7794