Corrigendum to “A Fatal Case of 3-Hydroxyisobutyryl-CoA Hydrolase Deficiency in a Term Infant With Severe High Anion Gap Acidosis and Review of the Literature”
Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
Taxonomy
TopicsMetabolism and Genetic Disorders · Diet and metabolism studies · Hyperglycemia and glycemic control in critically ill and hospitalized patients
S. Puvabanditsin, I. Lee, N. Cordero, K. Target, S. Y. Park, R. Mehta, “A Fatal Case of 3-Hydroxyisobutyryl-CoA Hydrolase Deficiency in a Term Infant With Severe High Anion Gap Acidosis and Review of the Literature,” Case Reports in Genetics, 2024, https://doi.org/10.1155/2024/8099373.
In the article, there is an error in Table 1, whereby the ethnicity of the reported patient of this case report in the final row is incorrect. The ethnicity should be India, not Pakistan. The correct Table 1 is shown below:
We apologize for this error.