Novel p.M96T variant of NRL and shRNA-based suppression and...

Clinical Genetics 2012 Vol. aop; Iss. aop

Novel p.M96T variant of NRL and shRNA-based suppression and replacement of NRL mutants associated with autosomal dominant retinitis pigmentosa

I Hernan, MJ Gamundi, E Borràs, M Maseras, B García-Sandoval, F Blanco-Kelly, C Ayuso, M Carballo
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Volume:
aop
Year:
2012
Language:
english
DOI:
10.1111/j.1399-0004.2011.01796.x
File:
PDF, 776 KB
english, 2012
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