Rapid aging: Biallelic POLR3A mutations cause neonatal progeroid syndrome

An international collaboration of scientists including researchers of the Institute of Human Genetics Göttingen have determined specific mutations in POLR3A as the genetic cause of [...]

Gene of the Month – September: MSL3

MSL (male specific lethal) factors commonly act in a protein complex to regulate chromatin-associated gene transcription. MSL3, one of these factors, is responsible for incorporation of MOF, a [...]