Atypical asymmetric lattice corneal dystrophy associated with a novel homozygous mutation (Val624Met) in the TGFBI gene

Por Afshari, Natalie A., Bahadur, Rosanna P., Eifrig, David E., Thogersen, Ida B., Enghild, Jan J., Klintworth, Gordon K.
Publicado em 2008