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Year : 2017 | Volume: 27 | Issue Number: 5 | Page: 402-405 CASE REPORTPrimary hyperoxaluria Type 1 with homozygosity for a double-mutated AGXT allele in a 2-year-old child Krishnamurthy S, Kartha G B, Venkateswaran V S, Prasannakumar M, Mahadevan S, Gowda M, Pelle A, Giachino D
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