Cockayne syndrome without typical clinical manifestations including neurologic abnormalities
- 1 October 1998
- journal article
- case report
- Published by Elsevier in Journal of the American Academy of Dermatology
- Vol. 39 (4) , 565-570
- https://doi.org/10.1016/s0190-9622(98)70005-2
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- A new UV-sensitive syndrome not belonging to any complementation groups of xeroderma pigmentosum or Cockayne syndrome: siblings showing biochemical characteristics of Cockayne syndrome without typical clinical manifestationsPublished by Elsevier ,2002
- Cockayne syndrome in two adult siblingsJournal of the American Academy of Dermatology, 1994
- Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cellsNucleic Acids Research, 1993
- Cockayne syndrome: Review of 140 casesAmerican Journal of Medical Genetics, 1992
- Evidence for detective repair of cyclobutane pyrimidine dimers with normal repair of other DNA photoproducts in a transcriptionally active gene transfected into Cockayne syndrome cellsMutation Research/DNA Repair, 1991
- Somatic Mosaicism for DNA Repair Capacity in Fibroblasts Derived from a Group A Xeroderma Pigmentosum PatientJournal of Investigative Dermatology, 1989
- Cockayne syndrome: Unusual neuropathological findings and review of the literatureAnnals of Neurology, 1979
- Cockayne's Syndrome Fibroblasts Have Increased Sensitivity to Ultraviolet Light But Normal Rates of Unscheduled DNA SynthesisJournal of Investigative Dermatology, 1978
- Cockayne's syndromeEuropean Journal of Pediatrics, 1970
- Dwarfism with retinal atrophy and deafnessArchives of Disease in Childhood, 1936