PAX7 nucleotide variants and the risk of non-syndromic orofacial clefts in the Polish population.
Agnieszka GaczkowskaBarbara BiedziakMargareta BudnerMałgorzata ZadurskaAgnieszka LasotaKamil K HozyaszJustyna DąbrowskaPiotr WójcickiAnna Szponar-ŻurowskaKacper ŻukowskiPaweł P JagodzińskiAdrianna MostowskaPublished in: Oral diseases (2019)
Our study confirmed that PAX7 is a strong candidate gene for nsCL/P. Nucleotide variants of this gene contribute to the etiology of nsCL/P in the homogenous Polish population.