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Article

Various phenotypic expressions of familial aniridia with a PAX6 mutation.

The British journal of ophthalmology - 1 Aug 1999

Negishi K, Azuma N, Yamada M

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 10636680
DOI: 10.1136/bjo.83.8.e987
PMCID: PMC1723133

Genes

PAX6

Provenance

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Related research

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Various phenotypic expressions of familial aniridia with a PAX6 mutation.PMID 10636680Read ↗

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Clinical and molecular aspects of congenital aniridia - A review of current concepts.Semantic proximity Read ↗

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PAX6 aniridia syndrome: clinics, genetics, and therapeutics.Semantic proximity Read ↗

A [c.566-2A>G] heterozygous mutation in the PAX6 gene causes aniridia with mild visual impairment.Semantic proximity Read ↗

The genetics of aniridia - simple things become complicated.Semantic proximity Read ↗

Congenital aniridia: etiology, manifestations and managementSemantic proximity Read ↗

A rare association of aniridia with conjunctival xerosis in two Indian siblings with PAX6 mutation.Semantic proximity Read ↗

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