PHADKE, A. K.; KUMBLE, A.; RAIKAR, P.; JACOB, M. Clinical and genetic characterization of neonatal non-ketotic hyperglycinemia: a rare case with SLC6A9 gene mutation. International Journal of Research in Medical Sciences, [S. l.], v. 13, n. 6, p. 2613–2616, 2025. DOI: 10.18203/2320-6012.ijrms20251653. Disponível em: https://www.msjonline.org/index.php/ijrms/article/view/14717. Acesso em: 30 sep. 2025.