MED12 mutation frequency in unselected sporadic uterine leiomyomas Hanna-Riikka Heinonen, M.B., Nanna S. Sarvilinna, M.D., Ph.D., Jari Sjöberg, M.D., Ph.D., Kati Kämpjärvi, M.Sc., Esa Pitkänen, Ph.D., Pia Vahteristo, Ph.D., Netta Mäkinen, M.Sc., Lauri A. Aaltonen, M.D., Ph.D.  Fertility and Sterility  Volume 102, Issue 4, Pages 1137-1142 (October 2014) DOI: 10.1016/j.fertnstert.2014.06.040 Copyright © 2014 American Society for Reproductive Medicine Terms and Conditions

Figure 1 Distribution of MED12 mutations in (A) consecutive and (B) unselected patient series. Missense mutations affecting different codons, in-frame deletions/insertion-deletions in exon 2 or in intron 1-exon 2 junction, and exon 1 mutations are shown separately. Codon 44 mutations are represented in more detail. Fertility and Sterility 2014 102, 1137-1142DOI: (10.1016/j.fertnstert.2014.06.040) Copyright © 2014 American Society for Reproductive Medicine Terms and Conditions