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Stanton, Chloe M, Borooah, Shyamanga, Drake, Camilla, Marsh, Joseph A, Campbell, Susan, Lennon, Alan, Soares, Dinesh C, Vallabh, Neeru A ORCID: 0000-0002-0109-4112, Sahni, Jayashree, Cideciyan, Artur V
et al (show 5 more authors) (2017) Novel pathogenic mutations in <i>C1QTNF5</i> support a dominant negative disease mechanism in late-onset retinal degeneration. SCIENTIFIC REPORTS, 7 (1). 12147-.

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