Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram (Opthalmic Genetics (2007) 28, (135-142))

S. Thiagalingam, T. L. McGee, R. G. Weleber, M. A. Sandberg, K. M. Trzupek, E. L. Berson, T. P. Dryja

Research output: Contribution to journalComment/debatepeer-review

Original languageEnglish (US)
Number of pages1
JournalOphthalmic Genetics
Issue number4
StatePublished - Oct 1 2007
Externally publishedYes

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Ophthalmology
  • Genetics(clinical)

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