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Article

Screening of the LTBP2 gene in a north Indian population with primary congenital glaucoma.

Molecular vision - 1 Jan 2013

Mohanty Kuldeep, Tanwar Mukesh, Dada Rima, Dada Tanuj

Abstract excerpt

PURPOSE: Primary congenital glaucoma (PCG), a severe form of glaucoma that presents early in life, is an autosomal recessive eye disorder that results from defects in anterior eye segment. Null mutations in LTBP2 were reported in patients with PCG in Pakistani and Iranian families. This study was aimed to identify the mutation profile of the LTBP2 gene in north Indian patients with PCG. METHODS: After ethical...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Open in PubMed Open full text

Identifiers

PMID: 23378721
PMCID: PMC3559091

Genes

LTBP2
FOXC1
MYOC

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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