Copyright
©The Author(s) 2021.
World J Clin Cases. Jan 16, 2021; 9(2): 436-444
Published online Jan 16, 2021. doi: 10.12998/wjcc.v9.i2.436
Published online Jan 16, 2021. doi: 10.12998/wjcc.v9.i2.436
Figure 1 Genetic testing of the isovaleryl-CoA dehydrogenase gene.
Sequence analysis of the isovaleryl-CoA dehydrogenase gene in the patient revealed the missense mutations, c.1193G>A (p.Arg398Gln) and c.1208A>G (p.Try403Cys).
- Citation: Wu F, Fan SJ, Zhou XH. Neonatal isovaleric acidemia in China: A case report and review of literature. World J Clin Cases 2021; 9(2): 436-444
- URL: https://www.wjgnet.com/2307-8960/full/v9/i2/436.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v9.i2.436