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Links from PubMed

Items: 5

1.

Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram.

Thiagalingam S, McGee TL, Weleber RG, Sandberg MA, Trzupek KM, Berson EL, Dryja TP.

Ophthalmic Genet. 2007 Sep;28(3):135-42. Erratum in: Ophthalmic Genet. 2007 Dec;28(4):231.

PMID:
17896311
2.

Genotype-phenotype correlation in a German family with a novel complex CRX mutation extending the open reading frame.

Paunescu K, Preising MN, Janke B, Wissinger B, Lorenz B.

Ophthalmology. 2007 Jul;114(7):1348-1357.e1. Epub 2007 Feb 22. Review.

PMID:
17320181
3.

Pathognomonic (diagnostic) ERGs. A review and update.

Vincent A, Robson AG, Holder GE.

Retina. 2013 Jan;33(1):5-12. doi: 10.1097/IAE.0b013e31827e2306. Review.

PMID:
23263253
4.

[Electroretinogram (ERG)].

Yamamoto S.

Nihon Rinsho. 1997 Mar;55 Suppl 1:443-5. Review. Japanese. No abstract available.

PMID:
9097646
5.

Two frameshift mutations of the double-stranded RNA-specific adenosine deaminase gene in Chinese pedigrees with dyschromatosis symmetrica hereditaria.

Liu Y, Xiao SX, Peng ZH, Lei XB, Wang JM, Li Y, Li XL.

Br J Dermatol. 2006 Aug;155(2):473-6. Review. No abstract available.

PMID:
16882194

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