A study published online in the May 3 edition of Developmental Cell reveals that researchers at the Weill Cornell Medical College and the Rockefeller University have identified the first gene, called Nkx2.5, which is associated with a rare condition called congenital asplenia, in which babies are born without a spleen.
View the original article here: Newborns With Missing Spleen – Genetic Link Identified – Medical News Today
