Associated Papers
Clinical and genetic analysis of ERCC8-Related cockayne syndrome: hepatic dysfunction as a biomarker, anhidrosis as a rare feature, and rehabilitation outcomes for ankle contractures.
Chen J et al.
Frontiers in Genetics, 2025
A compound heterozygous mutation of ERCC8 is responsible for a family with Cockayne syndrome.
Liu MW et al.
Molecular Biology Reports, 2024
Exome sequencing revealed a novel deletion in the ERCC8 gene in an Iranian family with Cockayne syndrome.
Mohammadi-Asl J et al.
Annals of Human Genetics, 2018
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