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Article

A clinical and molecular-genetic analysis of Chinese patients with lattice corneal dystrophy and novel Thr538Pro mutation in the TGFBI (BIGH3) gene.

Journal of genetics - 1 Apr 2006

Yu Ping, Gu Yangshun, Yang Yuehong, Yan Xiaoyi, Chen Lili, Ge Zhen, Qi Ming, Si Jianmin, Guo Lei

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 16809844
DOI: 10.1007/BF02728974

Genes

TGFBI

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A clinical and molecular-genetic analysis of Chinese patients with lattice corneal dystrophy and novel Thr538Pro mutation in the TGFBI (BIGH3) gene.PMID 16809844Read ↗

A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late-onset form of lattice corneal dystrophySemantic proximity Read ↗

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[A research on TGFBI gene mutations in Chinese families with corneal dystrophies].Semantic proximity Read ↗

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Lattice Corneal Dystrophy: a report of two cases in twin sisters due to 3 mutations (T1620C, C1416T, A1924G) in the TGFBI (BIGH3) gene.Semantic proximity Read ↗

Genetic and phenotypic investigation of a Chinese pedigree with lattice corneal dystrophy IIIB subtype.Semantic proximity Read ↗

[TGFBI gene mutations in three Chinese families with autosomal dominant corneal dystrophy].Semantic proximity Read ↗

Novel and known mutations of TGFBI, their genotype-phenotype correlation and structural modeling in 3 Chinese families with lattice corneal dystrophy.Semantic proximity Read ↗

TGFBI gene mutations analysis in Chinese families with corneal dystrophies.Semantic proximity Read ↗

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