Study on Rare Metabolic Disorder (Primary Hyperoxaluria Type 1) among Children: Perspectives to Genotyping and Outcome

Riyami, Mohamed S Al; Ghaithi, Badria Al; Hashmi, Nadia Al; Kalbani, Naifain Al

doi:10.9734/bpi/cdhr/v9/8613d

Challenges in Disease and Health Research Vol. 9 2021

DOI: 10.9734/bpi/cdhr/v9/8613d

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Study on Rare Metabolic Disorder (Primary Hyperoxaluria Type 1) among Children: Perspectives to Genotyping and Outcome

Mohamed S Al Riyami

Badria Al Ghaithi

Nadia Al Hashmi

et al.

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Study on Rare Metabolic Disorder (Primary Hyperoxaluria Type 1) among Children: Perspectives to Genotyping and Outcome

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