Proceedings of the National Academy of Sciences · 1987 · 144 citations · 22 references
Life SciencesGeneticsMolecular GeneticsCytogeneticsHuman GeneticsMedical GeneticsGenetic DisordersLoss Of HeterozygositySteroid Metabolism DisordersSteroidogenesis GeneticsSteroidogenic EnzymesX-chromosome InactivationCdna CloningDeletionsDna In Situ HybridizationGenomic DeletionsSomatic Cell Hybrid MappingSteroid Sulfatase ActivitySteroid Sulfatase DeficiencySteroid Sulfatases
We have isolated several cDNA clones from a lambda gt11 expression library by screening with antibodies prepared against the microsomal enzyme steroid sulfatase, which is deficient in classical X-chromosome-linked ichthyosis patients. One of these clones (p422) has been assigned by mapping with a somatic cell hybrid panel and by in situ hybridization to Xp22.3. Clone p422 therefore has a coincident localization with the previously identified locus for steroid sulfatase expression in the region of the X chromosome escaping from inactivation. Twelve steroid sulfatase-deficient patients, including eight cases of classical ichthyosis, were found to be deleted for genomic sequences detected by the clone.
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X-LINKED ICHTHYOSIS DUE TO STEROID-SULPHATASE DEFICIENCY
L J Shapiro, Roberta Weiss, Dianne Webster et al. · The Lancet · 1978 · 324 citations
M. Graziella Persico, Giuseppe Viglietto, G. Martini et al. · Nucleic Acids Research · 1986 · 246 citations · Full text