PRPH2-related retinal diseases: Broadening the clinical spectrum and describing a new mutation

1. Coco-Martin, R.M.
2. Sanchez-Tocino, H.T.
3. Desco, C.
4. Usategui-Martín, R.
5. Tellería, J.J.

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DOI: 10.3390/GENES11070773 GOOGLE SCHOLAR lock_openOpen access editor

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