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Article

TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients.

Investigative ophthalmology & visual science - 1 Jan 2005

Chakravarthi S V V Kalyana, Kannabiran Chitra, Sridhar Mittanamalli S, Vemuganti Geeta K

Abstract excerpt

PURPOSE: To identify mutations in the TGFBI gene in Indian patients with lattice corneal dystrophy (LCD) or granular corneal dystrophy (GCD) and to look for genotype-phenotype correlations. METHODS: Thirty-seven unrelated patients were studied, 18 with LCD and 19 with GCD. The diagnosis of LCD or GCD was made on the basis of clinical and/or histopathological evaluation. Exons and flanking intron sequences of the...

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Share to Corneal Dystrophies, Hereditary
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15623763
DOI: 10.1167/iovs.04-0440

Genes

TGFBI

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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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