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Cockayne syndrome-xeroderma pigmentosum complex with demyelination: A rare association

Usha Rani Singh1, Shujaath Asif, Peter Prasanth Kumar Kommu

  • 1Department of Pediatrics, Pondicherry Institute of Medical Sciences, Pondicherry, India.

Indian Journal of Human Genetics
|July 4, 2012
PubMed

Keywords:
Xeroderma pigmentosum–cockayne syndrome (XP–CS)demyelinationfacial phenotype

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