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Dive into the research topics of 'Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram'. Together they form a unique fingerprint.- Sort by
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Sureka Thiagalingam, Terri L. McGee, Richard G. Weleber, Michael A. Sandberg, Karmen M. Trzupek, Eliot L. Berson, Thaddeus P. Dryja
Research output: Contribution to journal › Article › peer-review