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bibliographicCitation Simonelli F, Testa F, Marini V, Interlandi E, Rossi S, Pognuz DR, Virgili G, Garrè C, Bandello F. Intrafamilial clinical heterogeneity associated with a novel mutation of the retinal degeneration slow/peripherin gene. Ophthalmic Res. 2007;39(5):255–9. doi: 10.1159/000108118. PMID: 17851265.
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title Intrafamilial Clinical Heterogeneity Associated with a Novel Mutation of the Retinal Degeneration Slow/Peripherin Gene
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