Mohamed S. AL RIYAMI; Badria Al GHAITHI; Nadia Al HASHMI; Naifain Al KALBANI. Study on Rare Metabolic Disorder (Primary Hyperoxaluria Type 1) among Children: Perspectives to Genotyping and Outcome. Challenges in Disease and Health Research Vol. 9, [S. l.], p. 5–13, 2021. DOI: 10.9734/bpi/cdhr/v9/8613D. Disponível em: https://stm.bookpi.org/CDHR-V9/article/view/2056. Acesso em: 11 jun. 2026.