Novel p.M96T variant of NRL and shRNA‐based suppression and replacement of NRL mutants associated with autosomal dominant retinitis pigmentosa
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I. Hernán | C. Ayuso | B. García-Sandoval | F. Blanco-Kelly | E. Borrás | M. Carballo | M. Gamundi | M. Maseras | B. García‐Sandoval