Axenfeld-Rieger syndrome-Reference-Cited by-同舟云学术

Axenfeld-Rieger syndrome

Published:2018-01-25 Issue:6 Volume:93 Page:1123-1130
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Seifi M.¹^ORCID,Walter M.A.¹

Affiliation:

1. Department of Medical Genetics, Faculty of Medicine and Dentistry; University of Alberta; Alberta, Edmonton Canada

Funder

Alberta Innovates Health Solutions

the Canadian Institute for Health Research

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.13148/fullpdf

Reference68 articles.

1. Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesis;Berry;Hum Mol Genet,2006

2. Embryotoxon corneaposterius;Axenfeld;Klin Monbl Augenheilkd,1920

3. Dysgenesis mesodermalis corneae et iridis;Rieger;Z Augenheilkd,1935

4. Axenfeld-Rieger syndrome and spectrum of PITX2 and FOXC1 mutations;Tümer;Eur J Hum Genet,2009

5. Molecular mechanisms of retinal ganglion cell degeneration in glaucoma and future prospects for cell body and axonal protection;Munemasa;Front Cell Neurosci,2012

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