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Identification of nine novel arylsulfatase a...
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