- Metabolite
- HMDB0002366 (Tiglylcarnitine)
- Biospecimen
- Blood
- Status
- Detected and Quantified
- Data source
- Referenced
- Concentration
- <0.0400 uM
- Age
- Not Specified
- Sex
- Not Specified
- Condition
- Normal
Comments
n=1. The name in the metabolite column seems to indicate multiple metabolites, so this row is probably not useful.
References
- Perez-Cerda C, Garcia-Villoria J, Ofman R, Sala PR, Merinero B, Ramos J, Garcia-Silva MT, Beseler B, Dalmau J, Wanders RJ, Ugarte M, Ribes A: 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency: an X-linked inborn error of isoleucine metabolism that may mimic a mitochondrial disease. Pediatr Res. 2005 Sep;58(3):488-91. [PubMed:16148061 ]