An Assessment of GUCA1C Variants in Primary Congenital Glaucoma

Emmanuelle Souzeau; Nicole Weisschuh; Jamie E Craig; Francesca Pasutto; Karl-Wilhelm Koch

doi:10.3390/genes12030359

An Assessment of GUCA1C Variants in Primary Congenital Glaucoma

Genes (Basel). 2021 Mar 2;12(3):359. doi: 10.3390/genes12030359.

Authors

Emmanuelle Souzeau¹, Nicole Weisschuh², Jamie E Craig¹, Francesca Pasutto³, Karl-Wilhelm Koch^{4

5}

Affiliations

¹ Department of Ophthalmology, Flinders University, Flinders Medical Centre, Bedford Park, SA 5042, Australia.
² Institute for Ophthalmic Research, Centre for Ophthalmology, University of Tübingen, 72076 Tübingen, Germany.
³ Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.
⁴ Department of Neuroscience, Division of Biochemistry, University of Oldenburg, 26129 Oldenburg, Germany.
⁵ Research Center for Neurosensory Sciences, University of Oldenburg, 26129 Oldenburg, Germany.

Abstract

In the special issue "Molecular Genetics of Retinal Dystrophies", Morales-Cámara and colleagues reported the association of a new candidate gene with primary congenital glaucoma (PCG) [...].

Keywords: GCAP3; GUCA1C; primary congenital glaucoma.

Publication types

Research Support, Non-U.S. Gov't
Comment

MeSH terms

Glaucoma* / genetics
Humans