AKTER, N. .; SHAMSAD, I. A. . Homozygous mutation of OCLN gene in Pseudo-TORCH Syndrome Type I : A Case Report. Bangladesh Journal of Child Health, [S. l.], v. 46, n. 2, p. 95–97, 2024. DOI: 10.3329/bjch.v46i2.72125. Disponível em: https://banglajol.info/index.php/BJCH/article/view/72125. Acesso em: 22 dec. 2024.