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Genetic analysis of patients with Fuchs endothelial corneal dystrophy in India

Genetic analysis of patients with Fuchs endothelial corneal dystrophy in India

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_4f2cb2782e9e40d89a9a126cd99c5c5c

Genetic analysis of patients with Fuchs endothelial corneal dystrophy in India

About this item

Full title

Genetic analysis of patients with Fuchs endothelial corneal dystrophy in India

Publisher

England: BioMed Central Ltd

Journal title

BMC ophthalmology, 2010-02, Vol.10 (1), p.3-3, Article 3

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

Mutations in COL8A2 gene which encodes the collagen alpha-2 (VIII) chain have been identified in both familial and sporadic cases of Fuchs endothelial corneal dystrophy (FECD). Heterozygous mutations in the SLC4A11 gene are also known to cause late-onset FECD. Therefore we screened for COL8A2, SLC4A11 gene variants in Indian FECD patients.
Eight...

Alternative Titles

Full title

Genetic analysis of patients with Fuchs endothelial corneal dystrophy in India

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_4f2cb2782e9e40d89a9a126cd99c5c5c

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_4f2cb2782e9e40d89a9a126cd99c5c5c

Other Identifiers

ISSN

1471-2415

E-ISSN

1471-2415

DOI

10.1186/1471-2415-10-3

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