Metachromatic leukodystrophy: a 12-bp deletion in exon 2 of the arylsulfatase A gene in a late infantile variant
- 1 September 1995
- journal article
- case report
- Published by Springer Nature in Human Genetics
- Vol. 96 (3) , 357-360
- https://doi.org/10.1007/bf00210424
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Molecular genetics of metachromatic leukodystrophyHuman Mutation, 1994
- Mutations in the arylsulfatase A pseudodeficiency allele causing metachromatic leukodystrophy.1991
- Molecular Basis of Different Forms of Metachromatic LeukodystrophyNew England Journal of Medicine, 1991
- Analysis of the accuracy and implications of simple methods for predicting the secondary structure of globular proteinsJournal of Molecular Biology, 1978
- Prediction of protein conformationBiochemistry, 1974