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.
| Autor: | Dutta, A. K.1, Paulose, B. K.2, Danda, S.1 sdanda@cmcvellore.ac.in, Alexander, S.2, Tamilarasi, V.2, Omprakash, S.1 |
|---|---|
| Zdroj: | Indian Journal of Nephrology. Jul/Aug2016, Vol. 26 Issue 4, p288-290. 3p. |
| Databáze: | Academic Search Ultimate |
| Externí odkaz: |
|