Exome Sequencing in a Swiss Childhood Glaucoma Cohort Reveals CYP1B1 and FOXC1 Variants as Most Frequent Causes-Reference-Cited by-同舟云学术

Exome Sequencing in a Swiss Childhood Glaucoma Cohort Reveals CYP1B1 and FOXC1 Variants as Most Frequent Causes

Published:2020-06-30 Issue:7 Volume:9 Page:47
ISSN:2164-2591
Container-title:Translational Vision Science & Technology
language:en
Short-container-title:Trans. Vis. Sci. Tech.

Author:

Lang Elena¹²,Koller Samuel²,Bähr Luzy²,Töteberg-Harms Marc¹,Atac David²,Roulez Françoise³,Bahr Angela⁴,Steindl Katharina⁴,Feil Silke²,Berger Wolfgang²⁵⁶,Gerth-Kahlert Christina¹

Affiliation:

1. Department of Ophthalmology, University Hospital Zurich, University of Zurich, Zurich, Switzerland

2. Institute of Medical Molecular Genetics, University of Zurich, Schlieren, Switzerland

3. Department of Ophthalmology, University Hospital Basel, Basel, Switzerland

4. Institute of Medical Genetics, University of Zurich, Zurich, Switzerland

5. Zurich Center for Integrative Human Physiology, University of Zurich, Zurich, Switzerland

6. Neuroscience Center Zurich, University and ETH Zurich, Zurich, Switzerland

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

Ophthalmology,Biomedical Engineering

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