A homozygous SIX6 mutation is associated with optic disc anomalies and macular atrophy and reduces retinal ganglion cell differentiation

Saved in:
Bibliographic Details
Published in:Clinical genetics 2015-02, Vol.87 (2), p.192-195
Main Authors: Yariz, K.O., Sakalar, Y.B., Jin, X., Hertz, J., Sener, E.F., Akay, H., Özbek, M.N., Farooq, A., Goldberg, J., Tekin, M.
Format: Article
Language:English
Subjects:
Adolescent
Atrophy - genetics
Atrophy - pathology
Cell Differentiation - genetics
Child
Child, Preschool
Female
Homeodomain Proteins - genetics
Homozygote
Humans
Macular Degeneration - genetics
Macular Degeneration - pathology
Male
Mutation
Optic Nerve Diseases - genetics
Optic Nerve Diseases - pathology
Retinal Ganglion Cells - pathology
Trans-Activators - genetics
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:
ISSN:0009-9163
1399-0004
DOI:10.1111/cge.12374