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

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Clinical genetics 2015-02, Vol.87 (2), p.192-195
Hauptverfasser:	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:	Artikel
Sprache:	eng
Schlagworte:	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
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!