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
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