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CASE REPORT

Primary 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

Year : 2017 | Volume:  27 | Issue Number:  5 | Page: 402-405



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Indian Journal of Nephrology
Published by Wolters Kluwer - Medknow
Online since 20th Sept '07