Novel frame shift mutation in ERCC6 leads to a severe form of Cockayne syndrome with postnatal growth failure and early death
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
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4. Adult-onset neurological degeneration in a patient with Cockayne syndrome and a null mutation in the CSB gene;Hashimoto;J Invest Dermatol,2008
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