A novel missense TGFBI variant p.(Ser591Phe) in a Finnish family with variant lattice corneal dystrophy

por Jaakkola, Aino Maaria, Järventausta, Petri J, Järvinen, Reetta-Stiina, Repo, Pauliina, Kivelä, Tero T, Turunen, Joni A
Publicado 2021