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Article

A novel TACSTD2 mutation identified in two Chinese brothers with gelatinous drop-like corneal dystrophy.

Molecular vision - 14 Aug 2009

Jing Yang, Liu Chun, Wang Liya

Abstract excerpt

PURPOSE: To identify the molecular defect causing gelatinous drop-like corneal dystrophy (GDLD) in two Chinese brothers and report the morphological evaluation of GDLD by laser scanning confocal microscopy and Fourier-domain optical coherence tomography (OCT). METHODS: Genetic analysis included p...

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Share to Antigens, Neoplasm
Share to Asian People
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Corneal Dystrophies, Hereditary

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Share to Tomography, Optical Coherence

Source

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Identifiers

PMID: 19693293
PMCID: PMC2728569

Genes

TACSTD2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19693293-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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