Ornithine Aminotransferase Deficiency in Differential Diagnosis of Neonatal Hyperammonemia: A Case with a Novel OAT Gene Mutation

Date
2016
Author
Kiykim, Ertuğrul
Cansever, Mehmet Serif
Zubarioglu, Tanyel
Zeybek, Cigdem Aktuglu
Metadata
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URI
http://hdl.handle.net/20.500.12627/63943
https://doi.org/10.1007/s12098-016-2077-3
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