Concepedia

Publication | Closed Access

Novel Mutations in the<i>KCNV2</i>Gene in Patients with Cone Dystrophy and a Supernormal Rod Electroretinogram

DOI

45

Citations

18

References

2007

Year

Sureka Thiagalingam, Terri L. McGee, Richard G. Weleber, Michael A. Sandberg, Karmen M Trzupek, Eliot L. Berson, Thaddeus P. Dryja
Ophthalmic Genetics

Abstract

KCNV2 mutations account for most if not all cases of cone dystrophy with a supernormal rod ERG.

References

YearCitations

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