Associated Papers
A family study implicates GBE1 in the etiology of autism spectrum disorder.
Fanjul-Fernández M et al.
Human Mutation, 2022
Discovery of rare ancestry-specific variants in the fetal genome that confer risk of preterm premature rupture of membranes (PPROM) and preterm birth.
Modi BP et al.
Bmc Medical Genetics, 2018
Select a paper to view details