Study on Rare Metabolic Disorder Primary Hyperoxaluria Type 1 among Children

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

View Book :- https://stm.bookpi.org/CDHR-V9/article/view/2056

#Metabolic_disorders #Primary_hyperoxaluria #AGXT_gene #genetic_mutations



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