Genomic strategies to understand causes of keratoconus-Reference-Cited by-同舟云学术

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Genomic strategies to understand causes of keratoconus

Published:2016-12-28 Issue:2 Volume:292 Page:251-269
ISSN:1617-4615
Container-title:Molecular Genetics and Genomics
language:en
Short-container-title:Mol Genet Genomics

Author:

Karolak Justyna A.,Gajecka Marzena

Funder

National Science Centre in Poland

Polish Ministry of Science and Higher Education

European Union under the European Social Fund

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00438-016-1283-z.pdf

Reference146 articles.

1. Abu A, Frydman M, Marek D et al (2008) Deleterious mutations in the Zinc-Finger 469 gene cause brittle cornea syndrome. Am J Hum Genet 82:1217–1222. doi: 10.1016/j.ajhg.2008.04.001

2. Abu-Amero KK, Kalantan H, Al-Muammar AM (2011) Analysis of the VSX1 gene in keratoconus patients from Saudi Arabia. Mol Vis 17:667–672

3. Abu-Amero KK, Azad TA, Kalantan H et al (2014) Mitochondrial sequence changes in keratoconus patients. Invest Ophthalmol Vis Sci 55:1706–1710. doi: 10.1167/iovs.14-13938

4. Abu-Amero KK, Helwa I, Al-Muammar A et al (2015a) Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population. J Negat Results Biomed 14:10. doi: 10.1186/s12952-015-0029-5

5. Abu-Amero KK, Helwa I, Al-Muammar A et al (2015b) Screening of the seed region of MIR184 in keratoconus patients from Saudi Arabia. BioMed Res Int 2015:604508. doi: 10.1155/2015/604508

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