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Number of items: 2.

2011

Tan, M.H.; (2011) Development of gene therapy for the treatment of retinal dystrophies caused by mutations in AIPL1. Doctoral thesis , UCL (University College London). Green open access
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2009

Tan, M. H.; Smith, A. J.; Pawlyk, B.; Xu, X.; Liu, X.; Bainbridge, J. B.; Basche, M.; ... Ali, R. R.; + view all (2009) Gene therapy for retinitis pigmentosa and Leber congenital amaurosis caused by defects in AIPL1: effective rescue of mouse models of partial and complete Aipl1 deficiency using AAV2/2 and AAV2/8 vectors. Human Molecular Genetics , 18 (12) pp. 2099-2114. 10.1093/hmg/ddp133. Green open access
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