[Congenital dystrophy: unilateral involvement in vitelliform retinal dystrophy or Best disease]

J Fr Ophtalmol. 2008 Jun;31(6 Pt 1):640-1. doi: 10.1016/s0181-5512(08)75471-8.

[Article in French]

Authors

I Meunier¹, S Ben Salah, C Arndt, C Hamel

Affiliation

¹ Centre National de Référence Maladies Rares, Affections sensorielles génétiques, CHRU de Montpellier, Hôpital Gui de Chauliac, Montpellier, France. [email protected]

PMID: 18772821
DOI: 10.1016/s0181-5512(08)75471-8

No abstract available

MeSH terms

Bestrophins
Chloride Channels / deficiency
Chloride Channels / genetics
Electrooculography*
Eye Proteins / genetics
Fluorescein Angiography*
Humans
Macular Degeneration / congenital*
Macular Degeneration / diagnosis
Macular Degeneration / genetics
Tomography, Optical Coherence*

Substances

BEST1 protein, human
Bestrophins
Chloride Channels
Eye Proteins