Ornithine Aminotransferase Deficiency in Differential...

Ornithine Aminotransferase Deficiency in Differential Diagnosis of Neonatal Hyperammonemia: A Case with a NovelOATGene Mutation

Zubarioglu, Tanyel, Kiykim, Ertugrul, Cansever, Mehmet Serif, Aktuglu Zeybek, Cigdem
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Volume:
83
Language:
english
Journal:
The Indian Journal of Pediatrics
DOI:
10.1007/s12098-016-2077-3
Date:
July, 2016
File:
PDF, 286 KB
english, 2016
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