Novel mutation and three other sequence variants segregating with phenotype at keratoconus 13q32 susceptibility locus-Reference-Cited by-同舟云学术

Novel mutation and three other sequence variants segregating with phenotype at keratoconus 13q32 susceptibility locus

Published:2011-11-02 Issue:4 Volume:20 Page:389-397
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Czugala Marta,Karolak Justyna A,Nowak Dorota M,Polakowski Piotr,Pitarque Jose,Molinari Andrea,Rydzanicz Malgorzata,Bejjani Bassem A,Yue Beatrice Y J T,Szaflik Jacek P,Gajecka Marzena

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/ejhg2011203.pdf

Reference65 articles.

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3. Ertan A, Muftuoglu O : Keratoconus clinical findings according to different age and gender groups. Cornea 2008; 27: 1109–1113.

4. Georgiou T, Funnell CL, Cassels-Brown A, O’Conor R : Influence of ethnic origin on the incidence of keratoconus and associated atopic disease in Asians and white patients. Eye (Lond) 2004; 18: 379–383.

5. Rabinowitz YS : The genetics of keratoconus. Ophthalmol Clin North Am 2003; 16: 607–620.

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