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Article

Identification of genome-wide copy number variations and a family-based association study of Avellino corneal dystrophy.

Ophthalmology - 1 Jul 2010

Bae Joon Seol, Cheong Hyun Sub, Chun Ji-Yong, Park Tae Joon, Kim Ji-On, Kim Eun Mi, Park Miey, Kim Dong-Joon, Lee Eun-Ju, Kim Eung Kweon, Lee Jong-Young, Shin Hyoung Doo

Abstract excerpt

OBJECTIVE: To determine the association of identified copy number variations (CNVs) in whole genome with the risk of Avellino corneal dystrophy (ACD) in a Korean population. DESIGN: Case-control study. PARTICIPANTS: A total of 146 patients with ACD and 226 control subjects. METHODS: A total of 19...

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PMID: 20202685
DOI: 10.1016/j.ophtha.2009.11.021

Genes

ACD

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20202685-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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