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pro vyhledávání: '"G. B Kartha"'
Autor:
Subramanian Mahadevan, V. S. Venkateswaran, Alessandra Pelle, M Prasannakumar, M Gowda, Sriram Krishnamurthy, G. B Kartha, Daniela Giachino
Publikováno v:
Indian Journal of Nephrology
Indian Journal of Nephrology, Vol 27, Iss 5, Pp 402-405 (2017)
Indian Journal of Nephrology, Vol 27, Iss 5, Pp 402-405 (2017)
Primary hyperoxaluria (PH) Type 1 is a rare, genetic disorder caused by deficiency of the liver enzyme alanine-glyoxylate aminotransferase, which is encoded by AGXT gene. We report a 2-year-old South Indian Tamil child with nephrocalcinosis due to PH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddb09b0bded572dcb55dd269f5d1e1ce
http://hdl.handle.net/2318/1647787
http://hdl.handle.net/2318/1647787
