[1]
Mohamed S. Al Riyami et al. 2021. Study on Rare Metabolic Disorder (Primary Hyperoxaluria Type 1) among Children: Perspectives to Genotyping and Outcome. Challenges in Disease and Health Research Vol. 9. (Jun. 2021), 5–13. DOI:https://doi.org/10.9734/bpi/cdhr/v9/8613D.