Copyright
©The Author(s) 2019.
World J Clin Cases. Dec 26, 2019; 7(24): 4355-4365
Published online Dec 26, 2019. doi: 10.12998/wjcc.v7.i24.4355
Published online Dec 26, 2019. doi: 10.12998/wjcc.v7.i24.4355
Figure 6 Genomic sequence of the patient.
Sequencing map of the actin alpha2 (ACTA2) gene showed a C-T heterozygous variation at nucleotide 536 in the coding region of the ACTA2 gene, causing 179 amino acid changes. No genetic mutations were found in her parents.
- Citation: Chen SN, Wang YQ, Hao CL, Lu YH, Jiang WJ, Gao CY, Wu M. Multisystem smooth muscle dysfunction syndrome in a Chinese girl: A case report and review of the literature. World J Clin Cases 2019; 7(24): 4355-4365
- URL: https://www.wjgnet.com/2307-8960/full/v7/i24/4355.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v7.i24.4355