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Year : 2016 | Volume:  26 | Issue Number:  4

CASE REPORT

Recurrent truncating mutations in alanine-glyoxylate aminotransferase gene in two South Indian families with primary hyperoxaluria type 1 causing later onset end-stage kidney disease

Dutta A K, Paulose B K, Danda S, Alexander S, Tamilarasi V, Omprakash S

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2019 Indian Journal of Nephrology
Published by Wolters Kluwer - Medknow
Online since 20th Sept '07