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