Association of polymorphisms in the intron of TCF4 gene to late-onset Fuchs endothelial corneal dystrophy: An Indian cohort study.

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Association of polymorphisms in the intron of TCF4 gene to late-onset Fuchs endothelial corneal dystrophy: An Indian cohort study.

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2017 nî lūn-bûn

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2017 թվականի հոկտեմբերին հրատարակված գիտական հոդված

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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name

Association of polymorphisms i ...... rophy: An Indian cohort study.

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Association of polymorphisms i ...... rophy: An Indian cohort study.

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Association of polymorphisms i ...... rophy: An Indian cohort study.

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Association of polymorphisms i ...... rophy: An Indian cohort study.

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Association of polymorphisms i ...... rophy: An Indian cohort study.

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Association of polymorphisms i ...... rophy: An Indian cohort study.

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P1476

Association of polymorphisms i ...... rophy: An Indian cohort study.

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P2093

Arokiasamy Tharigopala

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Bhavna S Rao

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Nagasamy Soumittra

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Rama Rajagopal

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Sudhir R Rachapalli

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P2860

Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American women

Haploview: analysis and visualization of LD and haplotype maps

E2-2 protein and Fuchs's corneal dystrophy

The effect of minor allele frequency on the likelihood of obtaining false positives.

Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p.

Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy.

Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy.

Missense mutations in the sodium borate cotransporter SLC4A11 cause late-onset Fuchs corneal dystrophy.

Differing roles for TCF4 and COL8A2 in central corneal thickness and fuchs endothelial corneal dystrophy.

Transethnic replication of association of CTG18.1 repeat expansion of TCF4 gene with Fuchs' corneal dystrophy in Chinese implies common causal variant

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931-935

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scholarly article

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10.4103/IJO.IJO_191_17

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English

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P478

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2017-10-01T00:00:00Z

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29044056

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P921

endothelium

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5678327

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