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Results: 4

Authors: VANDENHEUVEL LPWJ LUITEN B SMEITINK JAM RIJKVANANDEL JF HYLAND K STEENBERGENSPANJERS GCH JANSSEN RJT WEVERS RA
Citation: Lpwj. Vandenheuvel et al., A COMMON POINT MUTATION IN THE TYROSINE-HYDROXYLASE GENE IN AUTOSOMALRECESSIVE L-DOPA-RESPONSIVE DYSTONIA IN THE DUTCH POPULATION, Human genetics, 102(6), 1998, pp. 644-646

Authors: VERRIPS A STEENBERGENSPANJERS GCH LUYTEN JAFM WEVERS RA WOKKE JHJ GABREELS FJM WOLTHERS BG VANDENHEUVEL LPWJ
Citation: A. Verrips et al., EXON SKIPPING IN THE STEROL 27-HYDROXYLASE GENE LEADS TO CEREBROTENDINOUS XANTHOMATOSIS, Human genetics, 100(2), 1997, pp. 284-286

Authors: VERRIPS A STEENBERGENSPANJERS GCH LUYTEN JAFM VANDENHEUVEL LPWJ KEYSER A GABREELS FJM WEVERS RA
Citation: A. Verrips et al., 2 NEW MUTATIONS IN THE STEROL 27-HYDROXYLASE GENE IN 2 FAMILIES LEAD TO CEREBROTENDINOUS XANTHOMATOSIS, Human genetics, 98(6), 1996, pp. 735-737

Authors: LUYTEN JAFM WENINK PW STEENBERGENSPANJERS GCH WEVERS RA VANAMSTEL HKP DEJONG JGN VANDENHEUVEL LPWJ
Citation: Jafm. Luyten et al., METACHROMATIC LEUKODYSTROPHY - A 12-BP DELETION IN EXON-2 OF THE ARYLSULFATASE-A GENE IN A LATE INFANTILE VARIANT, Human genetics, 96(3), 1995, pp. 357-360
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