Gene therapy restores vision in rd1 mice after removal of a confounding mutation in Gpr179

por Nishiguchi, Koji M., Carvalho, Livia S., Rizzi, Matteo, Powell, Kate, Holthaus, Sophia-Martha kleine, Azam, Selina A., Duran, Yanai, Ribeiro, Joana, Luhmann, Ulrich F. O., Bainbridge, James W. B., Smith, Alexander J., Ali, Robin R.
Publicado 2015

The severity of retinal pathology in homozygous Crb1(rd8/rd8) mice is dependent on additional genetic factors

por Luhmann, Ulrich F.O., Carvalho, Livia S., Holthaus, Sophia-Martha kleine, Cowing, Jill A., Greenaway, Simon, Chu, Colin J., Herrmann, Philipp, Smith, Alexander J., Munro, Peter M.G., Potter, Paul, Bainbridge, James W.B., Ali, Robin R.
Publicado 2015