Biblio

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Journal Article

Cerrada V, García-López M, Moreno-Izquierdo A, Villaverde C, Zurita O, Martin-Merida MInmaculada, Arenas J, Ayuso C, M Gallardo E. Derivation of a human DOA iPSC line, IISHDOi006-A, with a mutation in the ACO2 gene: c.1999G>A; p.Glu667Lys. Stem Cell Res. 2019;40:101566.

Zurita-Díaz F, Ortuño-Costela MDel Carmen, Moreno-Izquierdo A, Galbis L, Millán JMaría, Ayuso C, Garesse R, M Gallardo E. Establishment of a human iPSC line, IISHDOi004-A, from a patient with Usher syndrome associated with the mutation c.2276G>T; p.Cys759Phe in the USH2A gene. Stem Cell Res. 2018;31:152-156.

Lukovic D, Castro AArtero, León M, Furió VDel Buey, Cortón M, Ayuso C, Erceg S. Generation of a human iPSC line from a patient with Leber congenital amaurosis caused by mutation in AIPL1. Stem Cell Res. 2018;33:151-155.

Castro AArtero, Long K, Bassett A, Machuca C, León M, Ávila-Fernandez A, Cortón M, Vidal-Puig T, Ayuso C, Lukovic D, et al. Generation of gene-corrected human induced pluripotent stem cell lines derived from retinitis pigmentosa patient with Ser331Cysfs*5 mutation in MERTK. Stem Cell Res. 2018;34:101341.

Lukovic D, Castro AArtero, Delgado ABelen Garc, Bernal Mde Los Ang, Pelaez NLuna, Lloret ADíez, Espejo RPerez, Kamenarova K, Sánchez LFernández, Cuenca N, et al. Human iPSC derived disease model of MERTK-associated retinitis pigmentosa. Sci Rep. 2015;5:12910.