Copyright
©The Author(s) 2021.
World J Clin Cases. Nov 16, 2021; 9(32): 10018-10023
Published online Nov 16, 2021. doi: 10.12998/wjcc.v9.i32.10018
Published online Nov 16, 2021. doi: 10.12998/wjcc.v9.i32.10018
Figure 2 Whole-exome sequencing showing the novel heterozygous mutation (c.
841 C>T) in MKRN3 detected in the profound. The same mutation was covered in A’s twin sister, her father and grandmother, but not A’s mother.
- Citation: Jiang LQ, Zhou YQ, Yuan K, Zhu JF, Fang YL, Wang CL. Rare mutation in MKRN3 in two twin sisters with central precocious puberty: Two case reports. World J Clin Cases 2021; 9(32): 10018-10023
- URL: https://www.wjgnet.com/2307-8960/full/v9/i32/10018.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v9.i32.10018