Intermediate levels of aryl sulfatase C in human leukocytes of female carriers for X-linked recessive ichthyosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Dermatology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF00455170.pdf
Reference19 articles.
1. Bedin M, Weil D, Fournier T, Cedard L, Frezal J (1981) Biochemical evidence for the non-inactivation of the steroid sulfatase locus in human placenta and fibroblasts. Hum Genet 59:256?258
2. Burns GRJ (1983) On the identity of aryl sulphatase C and steroid sulphatase. Hum Genet 65:169
3. Epstein EH, Leventhal ME (1981) Steroid sulfatase of human leukocytes and epidermis and the diagnosis of recessive X-linked ichthyosis. J Clin Invest 67:1257?1262
4. Epstein EH, Krauss RM, Shackleton CHL (1981) X-Linked ichthyosis: increased blood chloesterol sulfate and electrophoretic mobility of low-density lipoprotein. Science 214:659?660
5. Koppe JG, Marinkovic-Ilsen A, Rijken Y, De Groot WP, Jöbsis AC (1978) X-linked ichthyosis. A sulphatase deficiency. Arch Dis Child 53:803?806
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1. Mendelian Disorders of Cornification (MEDOC): The Ichthyoses;Harper's Textbook of Pediatric Dermatology;2011-05-24
2. Laboratory Tests for Ichthyosis;Dermatologic Clinics;1994-01
3. Correction of Steroid Sulfatase Deficiency by Gene Transfer into Basal Cells of Tissue-Cultured Epidermis from Patients with Recessive X-Linked Ichthyosis;Experimental Cell Research;1993-12
4. A fluorimetric assay of steroid sulphatase in leukocytes: Evidence for two genetically different enzymes with arylsulphatase C activity;Journal of Inherited Metabolic Disease;1989-09
5. Gene diagnosis in X-linked ichthyosis;Archives of Dermatological Research;1989-01
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