Copyright
©The Author(s) 2022.
World J Clin Cases. Dec 6, 2022; 10(34): 12761-12767
Published online Dec 6, 2022. doi: 10.12998/wjcc.v10.i34.12761
Published online Dec 6, 2022. doi: 10.12998/wjcc.v10.i34.12761
Figure 2 Whole-exome sequencing.
Red box indicates mutation site. A: PMFBP1 NM_031293.3: c.414+1G>T (p.?); B: PMFBP1 NM_031293.3: c.393del (p.C132Afs*3).
- Citation: Deng TQ, Xie YL, Pu JB, Xuan J, Li XM. Compound heterozygous mutations in PMFBP1 cause acephalic spermatozoa syndrome: A case report. World J Clin Cases 2022; 10(34): 12761-12767
- URL: https://www.wjgnet.com/2307-8960/full/v10/i34/12761.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v10.i34.12761