Mutational Analysis of an X-Linked Adrenoleukodystrophy (ALD) Patient with Detectable ALD Protein
- 1 December 1996
- journal article
- case report
- Published by Wiley in Annals of the New York Academy of Sciences
- Vol. 804 (1) , 756-759
- https://doi.org/10.1111/j.1749-6632.1996.tb18692.x
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Identification of mutations in the putative ATP-binding domain of the adrenoleukodystrophy gene.Journal of Clinical Investigation, 1994
- Adrenoleukodystrophy and other peroxisomal diseasesCurrent Opinion in Genetics & Development, 1994
- Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transportersNature, 1993
- Adrenoleukodystrophy: Phenotypic variability and implications for therapyJournal of Inherited Metabolic Disease, 1992
- Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells.Proceedings of the National Academy of Sciences, 1981