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

K. O. Yariz; Y. B. Sakalar; X. Jin; J. Hertz; E. F. Sener; H. Akay; M. N. Özbek; A. Farooq; J. Goldberg; M. Tekin

doi:10.1111/cge.12374

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

K. O. Yariz, Y. B. Sakalar, X. Jin, J. Hertz, E. F. Sener, H. Akay, M. N. Özbek, A. Farooq, J. Goldberg, M. Tekin

Research output: Contribution to journal › Letter › peer-review

Original language	English (US)
Pages (from-to)	192-195
Number of pages	4
Journal	Clinical Genetics
Volume	87
Issue number	2
DOIs	https://doi.org/10.1111/cge.12374
State	Published - Feb 1 2015

ASJC Scopus subject areas

Genetics
Genetics(clinical)

Access to Document

10.1111/cge.12374

Cite this

A homozygous SIX6 mutation is associated with optic disc anomalies and macular atrophy and reduces retinal ganglion cell differentiation. / Yariz, K. O.; Sakalar, Y. B.; Jin, X.; Hertz, J.; Sener, E. F.; Akay, H.; Özbek, M. N.; Farooq, A.; Goldberg, J.; Tekin, M.

In: Clinical Genetics, Vol. 87, No. 2, 01.02.2015, p. 192-195.

Research output: Contribution to journal › Letter › peer-review

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AU - Tekin, M.

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