The role of EMX2 in uterine development

Reflections on “Nonsense mutation of EMX2 is potential causative for uterus didelphysis: first molecular explanation for incomplete Mullerian fusion (IMF)” by Liu et al.

Authors

Hugh S. Taylor, M.D.

Volume 103, Issue 3, Pages 633-634

Abstract

Reflections on “Nonsense mutation of EMX2 is potential causative for uterus didelphysis: first molecular explanation for incomplete Mullerian fusion (IMF)” by Liu et al.

Read the full text at: http://www.fertstert.org/article/S0015-0282(15)00046-1/fulltext