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Article

Heterozygous coding ZNF469 variants enriched in New Zealand patients with isolated keratoconus.

Investigative ophthalmology & visual science - 8 Sept 2014

De Baere Elfride

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PMID: 25201924
DOI: 10.1167/iovs.14-15486

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Heterozygous coding ZNF469 variants enriched in New Zealand patients with isolated keratoconus.PMID 25201924Read ↗

Enrichment of pathogenic alleles in the brittle cornea gene, ZNF469, in keratoconus.Semantic proximity Read ↗

Novel Zinc Finger Protein Gene 469 (ZNF469) Variants in Advanced Keratoconus.Semantic proximity Read ↗

Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis of rare ZNF469 variants in familial keratoconus.Semantic proximity Read ↗

Rare, Potentially Pathogenic Variants in ZNF469 Are Not Enriched in Keratoconus in a Large Australian Cohort of European Descent.Semantic proximity Read ↗

Evidence against ZNF469 being causative for keratoconus in Polish patients.Semantic proximity Read ↗

Brittle cornea without clinically-evident extraocular findings in an adult harboring a novel homozygous ZNF469 mutation.Semantic proximity Read ↗

Identification of seven novel ZNF469 mutations in keratoconus patients in a Han Chinese population.Semantic proximity Read ↗

Mutations in the zinc finger protein gene, ZNF469, contribute to the pathogenesis of keratoconus.Semantic proximity Read ↗

Whole-exome sequencing in familial keratoconus: the challenges of a genetically complex disorder.Semantic proximity Read ↗

Biallelic novel variants in ZNF469 causing Brittle Cornea Syndrome 1: a detailed report of an Indian patient.Semantic proximity Read ↗

Whole exome sequencing highlights variants in association with Keratoconus in Jordanian families.Semantic proximity Read ↗

Genetic associations for keratoconus: a systematic review and meta-analysis.Semantic proximity Read ↗

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