Article
Identification of nine novel arylsulfatase a (ARSA) gene mutations in patients with metachromatic leukodystrophy (MLD).
Human mutation - 1 Nov 2003
Eng Barry, Nakamura Lisa N, O'Reilly Natasha, Schokman Natasha, Nowaczyk Magorzata M J, Krivit William, Waye John S
Abstract excerpt
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...
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