1.
Mohamed S. Al Riyami, Badria Al Ghaithi, Nadia Al Hashmi and Naifain Al Kalbani. Study on Rare Metabolic Disorder (Primary Hyperoxaluria Type 1) among Children: Perspectives to Genotyping and Outcome. CDHR-V9 [Internet]. 2021 Jun. 30 [cited 2026 Jun. 11];:5-13. Available from: https://stm.bookpi.org/CDHR-V9/article/view/2056