Carriers with functional null mutations in LAMA3 have localized enamel abnormalities due to haploinsufficiency
Gostyńska, Katarzyna B, Yan Yuen, Wing, Pasmooij, Anna Maria Gerdina, Stellingsma, Cornelius, Pas, Hendri H, Lemmink, Henny, Jonkman, Marcel FLanguage:
english
Journal:
European Journal of Human Genetics
DOI:
10.1038/ejhg.2016.136
Date:
November, 2016
File:
PDF, 1.03 MB
english, 2016