Metachromatic leukodystrophy: a 12-bp deletion in exon 2 of the arylsulfatase A gene in a late infantile variant.

J.A.F.M. Luyten, P.W. Wenink, G.C.H. Steenbergen, R.A. Wevers, H. Ploos, J.G.N. de Jong, L.P.W.J. van den Heuvel

    Research output: Contribution to journalArticleAcademicpeer-review

    13 Citations (Scopus)
    Original languageEnglish
    Pages (from-to)357-360
    JournalHuman Genetics
    Volume96
    DOIs
    Publication statusPublished - 1995

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