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

No abstract is available for this paper.

• Publication year

  2016

• Venue

  Indian Journal of Pediatrics

• Publication date

  2016-04-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.1007/s12098-016-2077-3PMID 27037922
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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