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Article

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

Indian journal of pediatrics - 1 Jul 2016

Zubarioglu Tanyel, Kiykim Ertugrul, Cansever Mehmet Serif, Aktuglu Zeybek Cigdem

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Identifiers

PMID: 27037922
DOI: 10.1007/s12098-016-2077-3

Genes

OAT

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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