
|Articles|March 21, 2008
Cockayne Syndrome Linked to Ancient Genetic Activity
Cockayne syndrome, an especially severe type of progeria often caused by mutations in the CSB gene, may be linked to a fusion protein that dates back in primates at least 43 million years, according to research published online March 21 in PLoS Genetics.
Advertisement
Newsletter
Access practical, evidence-based guidance to support better care for our youngest patients. Join our email list for the latest clinical updates.
Advertisement
Latest CME
Advertisement
Advertisement
Trending on Contemporary Pediatrics
1
Genomic sequencing may transform newborn screening
2
Kathryn M. Stephenson, MD, MA, discusses GLP-1 RA decisions for pediatric obesity
3
AAP calls for system-level changes to improve children’s digital media environments
4
AAP updates guidance on therapeutic hypothermia for neonatal hypoxic-ischemic encephalopathy
5






