POLR3GL

Publications

Beauregard-Lacroix E et al. A variant of neonatal progeroid syndrome, or Wiedemann-Rautenstrauch syndrome, is associated with a nonsense variant in POLR3GL. Eur J Hum Genet. 2020;28(4):461-468. PMID: 31695177.

Terhal P et al. Biallelic variants in POLR3GL cause endosteal hyperostosis and oligodontia. Eur J Hum Genet. 2020;28(1):31-39. PMID: 31089205.