H. Kremer, E. Van-wijk, T. Marker, U. Wolfrum, and R. Roepman, Usher syndrome: molecular links of pathogenesis, proteins and pathways, Hum. Mol. Genet, vol.15, issue.2, pp.262-270, 2006.

E. Lenassi, A. Vincent, Z. Li, Z. Saihan, A. J. Coffey et al., A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants, Eur. J. Hum. Genet, vol.23, issue.10, pp.1318-1327, 2015.

K. Takahashi, K. Tanabe, M. Ohnuki, M. Narita, T. Ichisaka et al., Induction of pluripotent stem cells from adult human fibroblasts by defined factors, Cell, vol.131, issue.5, pp.861-872, 2007.

S. Torriano, N. Erkilic, V. Faugère, K. Damodar, C. P. Hamel et al., Pathogenicity of a novel missense variant associated with choroideremia and its impact on gene replacement therapy, Hum. Mol. Genet, vol.26, issue.18, pp.3573-3584, 2017.