Figure 2 .

MommeD12 and MommeD38 have mutations in eIF3h. (A) Schematic of the eIF3h protein structure and positions of point mutations. The point mutation in MommeD12 causes skipping of exon 5. The MommeD38 mutation introduces a premature stop codon at amino acid 291, a highly conserved region of the protein. (B) Quantitative real-time RT-PCR analysis for eIF3h normalized to Hprt. The graph shows the mean ± SEM for four testes samples of each genotype. All reactions were performed in triplicate. Student t-test; *P < 0.05.