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Human iPSC-derived RPE and retinal organoids reveal impaired alternative splicing of genes involved in pre-mRNA splicing in PRPF31 autosomal dominant retinitis pigmentosa.

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Mozaffari-Jovin,  S.
Department of Cellular Biochemistry, MPI for biophysical chemistry, Max Planck Society;

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Lührmann,  R.
Department of Cellular Biochemistry, MPI for biophysical chemistry, Max Planck Society;

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Lako, M., Buskin, A., Zhu, L., Chichagova, V., Basu, B., Mozaffari-Jovin, S., et al. (2018). Human iPSC-derived RPE and retinal organoids reveal impaired alternative splicing of genes involved in pre-mRNA splicing in PRPF31 autosomal dominant retinitis pigmentosa. Investigative Ophthalmology and Visual Science, 59(9): 1563.


Cite as: https://hdl.handle.net/21.11116/0000-0002-47B1-6
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