Results 201 to 208 of about 9,462 (208)

Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment

American Journal of Medical Genetics, Part A, 2011
Nanna Dahl Rendtorff, Lars Hansen
exaly  

[Benign autosomal dominant hereditary optic atrophy].

Bulletin des societes d'ophtalmologie de France, 1986
P, Verin, P, Comte
openaire   +1 more source

Retinal vessel diameters decrease with macular ganglion cell layer thickness in autosomal dominant optic atrophy and in healthy subjects

Acta Ophthalmologica, 2014
Michael Larsen
exaly  

Analysis of opa1 isoforms expression and apoptosis regulation in autosomal dominant optic atrophy (ADOA) patients with mutations in the opa1 gene

Journal of the Neurological Sciences, 2015
Maria TERESA Dotti, Gian Nicola Gallus, Jlenia Brunetti   +2 more
exaly  

Optic Atrophy, Autosomal Dominant, Kjer Type

2012
openaire   +1 more source

Thickness mapping of individual retinal layers and sectors by Spectralis SD‐OCT in Autosomal Dominant Optic Atrophy

Acta Ophthalmologica, 2018
Nihada Ćorajević, Michael Larsen
exaly  

Colour vision in a pedigree with autosomal dominant optic atrophy.

Modern problems in ophthalmology, 1976
N, Ohba, P M, Imamura, T, Tanino
openaire   +1 more source

Optic Atrophy 3, Autosomal Dominant (OPA3)

openaire   +1 more source