Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndrome.
Gelila YitsegeBethany A StokesJulia A SabatinoKelsey F SugrueGabor BanyaiElizabeth M ParonettBeverly A KarpinskiThomas M MaynardAnthony-S LaMantiaIrene E ZohnPublished in: Birth defects research (2020)
Our studies demonstrate that variations in maternal vitamin A intake can influence the incidence and severity of phenotypes in a mouse model 22q11.2 deletion syndrome.