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, Richard Weleber, M. A. Sandberg, K. M. Trzupek, E. L. Berson, T. P. Dryja

Research output: Contribution to journalArticle

Original languageEnglish (US)
Pages (from-to)231
Number of pages1
JournalOphthalmic Genetics
Volume28
Issue number4
DOIs
StatePublished - Oct 2007
Externally publishedYes

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Mutation
Genes

ASJC Scopus subject areas

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

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Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram (Opthalmic Genetics (2007) 28, (135-142)). / Thiagalingam, S.; McGee, T. L.; Weleber, Richard; Sandberg, M. A.; Trzupek, K. M.; Berson, E. L.; Dryja, T. P.

In: Ophthalmic Genetics, Vol. 28, No. 4, 10.2007, p. 231.

Research output: Contribution to journalArticle

Thiagalingam, S. ; McGee, T. L. ; Weleber, Richard ; Sandberg, M. A. ; Trzupek, K. M. ; Berson, E. L. ; Dryja, T. P. / Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram (Opthalmic Genetics (2007) 28, (135-142)). In: Ophthalmic Genetics. 2007 ; Vol. 28, No. 4. pp. 231.
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