Adult-onset carnitine palmitoyl transferase II (CPT II) deficiency presenting with rhabdomyolysis and acute kidney injury
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Earth and Planetary Sciences,General Environmental Science
Link
https://link.springer.com/content/pdf/10.1007/s13730-023-00804-8.pdf
Reference25 articles.
1. Thuillier L, et al. Correlation between genotype, metabolic data, and clinical presentation in carnitine palmitoyltransferase 2 (CPT2) deficiency. Hum Mutat. 2003;21(5):493–501.
2. Oey NA, et al. Long-chain fatty acid oxidation during early human development. Pediatr Res. 2005;57(6):755–9.
3. Houten SM, Wanders RJ. A general introduction to the biochemistry of mitochondrial fatty acid β-oxidation. J Inherit Metab Dis. 2010;33(5):469–77.
4. Bonnefont J-P, et al. Carnitine palmitoyltransferase deficiencies. Mol Genet Metab. 1999;68(4):424–40.
5. Longo, N., C. Amat di San Filippo, and M. Pasquali. Disorders of carnitine transport and the carnitine cycle. in American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 2006. Wiley Online Library
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1. Myopathic Carnitine Palmitoyltransferase II (CPT II) Deficiency: A Rare Cause of Acute Kidney Injury and Cardiomyopathy;Cureus;2023-10-06
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