Myopia disease mouse models: a missense point mutation (S673G) and a protein-truncating mutation of the Zfp644 mimic human disease phenotype-Reference-Cited by-同舟云学术

Myopia disease mouse models: a missense point mutation (S673G) and a protein-truncating mutation of the Zfp644 mimic human disease phenotype

Published:2019-02-21 Issue:1 Volume:9 Page:
ISSN:2045-3701
Container-title:Cell & Bioscience
language:en
Short-container-title:Cell Biosci

Author:

Szczerkowska Katarzyna I.,Petrezselyova Silvia,Lindovsky Jiri,Palkova Marcela,Dvorak Jan,Makovicky Peter,Fang Mingyan,Jiang Chongyi,Chen Lingyan,Shi Mingming,Liu Xiao,Zhang Jianguo,Kubik-Zahorodna Agnieszka,Schuster Bjoern,Beck Inken M.,Novosadova Vendula,Prochazka Jan,Sedlacek Radislav^ORCID

Funder

Ministerstvo Školství, Mládeže a Tělovýchovy

Akademie Věd České Republiky

Grantová Agentura České Republiky

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology

Link

http://link.springer.com/content/pdf/10.1186/s13578-019-0280-4.pdf

Reference51 articles.

1. Lopes MC, Andrew T, Carbonaro F, Spector TD, Hammond CJ. Estimating heritability and shared environmental effects for refractive error in twin and family studies. Invest Ophthalmol Vis Sci. 2009;50(1):126–31.