Copyright
©The Author(s) 2022.
World J Clin Cases. Jan 21, 2022; 10(3): 1056-1066
Published online Jan 21, 2022. doi: 10.12998/wjcc.v10.i3.1056
Published online Jan 21, 2022. doi: 10.12998/wjcc.v10.i3.1056
Figure 1 Gene detection results for case 1.
A: c.1068dup T (p.D357_D358delin sX) mutant type; B: c.1068dup T (p.D357_D358delin sX) wild type; C: c.40G>C (p.G14R) mutant type; D: c.40G>C (p.G14R) wild type.
- Citation: Wu WJ, Sun SZ, Li BG. Congenital muscular dystrophy caused by beta1,3-N-acetylgalactosaminyltransferase 2 gene mutation: Two case reports. World J Clin Cases 2022; 10(3): 1056-1066
- URL: https://www.wjgnet.com/2307-8960/full/v10/i3/1056.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v10.i3.1056