Associated Papers
A possible cranio-oro-facial phenotype in Cockayne syndrome.
Bloch-Zupan A et al.
Orphanet Journal of Rare Diseases, 2013
Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome.
Laugel V et al.
Human Mutation, 2010
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