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

doi:10.1080/13816810701769118

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

Ophthalmology

Research output: Contribution to journal › Comment/debate

Original language	English (US)
Number of pages	1
Journal	Ophthalmic Genetics
Volume	28
Issue number	4
DOIs	https://doi.org/10.1080/13816810701769118
State	Published - Oct 1 2007

ASJC Scopus subject areas

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

Access to Document

10.1080/13816810701769118

Cite this

Thiagalingam, S., McGee, T. L., Weleber, R. G., Sandberg, M. A., Trzupek, K. M., Berson, E. L., & Dryja, T. P. (2007). Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram (Opthalmic Genetics (2007) 28, (135-142)). Ophthalmic Genetics, 28(4). https://doi.org/10.1080/13816810701769118

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, R. G.; Sandberg, M. A.; Trzupek, K. M.; Berson, E. L.; Dryja, T. P.

In: Ophthalmic Genetics, Vol. 28, No. 4, 01.10.2007.

Research output: Contribution to journal › Comment/debate

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