Resequencing of candidate genes for Keratoconus reveals a role for Ehlers–Danlos Syndrome genes-Reference-Cited by-同舟云学术

Resequencing of candidate genes for Keratoconus reveals a role for Ehlers–Danlos Syndrome genes

Published:2021-03-19 Issue:12 Volume:29 Page:1745-1755
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Fransen Erik,Valgaeren Hanne,Janssens Katleen,Sommen Manou,De Ridder Raphael^ORCID,Vandeweyer Geert,Bisceglia Luigi,Soler Vincent,Hoischen Alexander,Mortier Geert,Malecaze François,Koppen Carina^ORCID,Van Camp Guy^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

https://www.nature.com/articles/s41431-021-00849-2.pdf

Reference44 articles.

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2. Godefrooij DA, de Wit GA, Uiterwaal CS, Imhof SM, Wisse RP. Age-specific incidence and prevalence of keratoconus: a nationwide registration study. Am J Ophthalmol. 2017;175:169–72.

3. Tuft SJ, Hassan H, George S, Frazer DG, Willoughby CE, Liskova P. Keratoconus in 18 pairs of twins. Acta Ophthalmol. 2012;90:e482–6.

4. Wang Y, Rabinowitz YS, Rotter JI, Yang H. Genetic epidemiological study of keratoconus: evidence for major gene determination. Am J Med Genet. 2000;93:403–9.

5. Szczotka-Flynn L, Slaughter M, McMahon T, Barr J, Edrington T, Fink B, et al. Disease severity and family history in keratoconus. Br J Ophthalmol. 2008;92:1108–11.

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