Copyright
©The Author(s) 2025.
World J Clin Cases. May 26, 2025; 13(15): 101272
Published online May 26, 2025. doi: 10.12998/wjcc.v13.i15.101272
Published online May 26, 2025. doi: 10.12998/wjcc.v13.i15.101272
Figure 5 Sanger sequencing DNA chromatogram in MYH7 gene of the pedigree.
A: II-4; B: III-4; C: IV-3; D: II-7. Subjects (II-4, III-4 and IV-3) all presented with a heterozygous missense mutation (c.746G>A, p.R249Q). Subject II-7 was normal.
- Citation: Hong Y, Fan Z, Guo Y, Ma HH, Zeng SZ, Xi HT, Yang J, Luo K, Luo R, Li XP. MYH7 mutation in a pedigree with familial dilated hypertrophic cardiomyopathy: A case report and review of literature. World J Clin Cases 2025; 13(15): 101272
- URL: https://www.wjgnet.com/2307-8960/full/v13/i15/101272.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v13.i15.101272