Gene therapy restores vision and delays degeneration in the CNGB1 −/− mouse model of retinitis pigmentosa

By Koch Susanne   Sothilingam Vithiyanjali   Garcia Garrido Marina   Tanimoto Naoyuki   Becirovic Elvir   Koch Fred   Seide Christina   Beck Susanne C.   Seeliger Mathias W.   Biel Martin   Mühlfriedel Regine   Michalakis Stylianos  

Human Molecular Genetics, Vol. 21, Iss. 20, 2012-10 ,pp. : 4486-4496

Oxford University Press

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Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13)

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Human Molecular Genetics, Vol. 10, Iss. 15, 2001-07 ,pp. : 1555-1562

Oxford University Press

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A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss

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Human Genetics, Vol. 121, Iss. 2, 2007-04 ,pp. : 203-211

Springer Publishing Company

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Murine model of autosomal dominant retinitis pigmentosa generated by targeted deletion at codon 307 of the rds –peripherin gene

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Human Molecular Genetics, Vol. 11, Iss. 9, 2002-05 ,pp. : 1005-1016

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Pharmacological manipulation of gain-of-function and dominant-negative mechanisms in rhodopsin retinitis pigmentosa

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Human Molecular Genetics, Vol. 17, Iss. 19, 2008-10 ,pp. : 3043-3054

Oxford University Press

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