Ornithine Aminotransferase Deficiency in Differential Diagnosis of Neonatal Hyperammonemia: A Case with a Novel OAT Gene Mutation
Crossref DOI link: https://doi.org/10.1007/s12098-016-2077-3
Published Online: 2016-04-01
Published Print: 2016-07
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Zubarioglu, Tanyel
Kiykim, Ertugrul
Cansever, Mehmet Serif
Aktuglu Zeybek, Cigdem
Funding for this research was provided by:
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Text and Data Mining valid from 2016-04-01