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Article

Analysis of SLC4A11, ZEB1, LOXHD1, COL8A2 and TCF4 gene sequences in a multi-generational family with late-onset Fuchs corneal dystrophy.

International journal of molecular medicine - 1 Jun 2016

Tang Hui, Zhang Wen, Yan Xin-Min, Wang Lin-Ping, Dong Hong, Shou Tao, Lei Huo, Guo Qiang

Abstract excerpt

The aim of the present study was to determine the genetic basis of a multi-generational family with late-onset (LO) Fuchs corneal dystrophy (FCD). Five FCD causal genes [solute carrier family 4, sodium borate transporter, member 11 (SLC4A11), zinc finger E-box binding homeobox 1 (ZEB1), lipoxygenase homology domains 1 (LOXHD1), collagen, type VIII, alpha 2 (COL8A2) and transcription factor 4 (TCF4)], previously...

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Source

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Identifiers

PMID: 27121161
DOI: 10.3892/ijmm.2016.2570
PMCID: PMC4866966

Genes

LOXHD1
ZEB1
TCF4

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Analysis of SLC4A11, ZEB1, LOXHD1, COL8A2 and TCF4 gene sequences in a multi-generational family with late-onset Fuchs corneal dystrophy.PMID 27121161Read ↗

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