Metachromatic leukocystrophy: a 12-bp deletion in exon 2 of the Arylsulfatase A gene in a late infantile variant.
Publication year
1995Source
Human Genetics, 96, (1995), pp. 357-360ISSN
Publication type
Article / Letter to editor

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Organization
Neurology
Paediatrics - OUD tm 2017
Journal title
Human Genetics
Volume
vol. 96
Page start
p. 357
Page end
p. 360
Subject
Lysosomal and neurometabolic diseases; Lysosomale en neurometabole ziektenThis item appears in the following Collection(s)
- Academic publications [232014]
- Faculty of Medical Sciences [89012]
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