FATEMA, K.; RAHMAN, M. M.; AKHTER, S. Cockayne Syndrome with ERCC8 Gene Mutation: A Case Report. Bangladesh Journal of Child Health, [S. l.], v. 44, n. 3, p. 181–183, 2021. DOI: 10.3329/bjch.v44i3.52713. Disponível em: https://banglajol.info/index.php/BJCH/article/view/52713. Acesso em: 1 sep. 2024.