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Article

The association of a single nucleotide polymorphism in the promoter region of the LAMA1 gene with susceptibility to Chinese high myopia.

Molecular vision - 22 Apr 2011

Zhao Yan Yan, Zhang Feng Ju, Zhu Si Quan, Duan Hui, Li Yang, Zhou Zhong Jun, Ma Wen Xian, Li Wang Ning

Abstract excerpt

PURPOSE: High myopia is a severe hereditary ocular disease leading to blindness. LAMA1 (alpha subunit of laminin) is a promising candidate gene for high myopia present in the MYP2 (myopia 2) region. The purpose of this study was to determine if high myopia is associated with single nucleotide polymorphism (SNP) variants in LAMA1 in Chinese subjects. METHODS: Ninety-seven Chinese subjects with high myopia and...

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Source

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Identifiers

PMID: 21541277
PMCID: PMC3084244

Genes

LAMA1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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