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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

Year : 2016 | Volume: 26 | Issue Number: 4 | Page: 288-290

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