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Article

Homozygous Nonsense Mutation in the FOXE3 Gene as a Cause of Congenital Primary Aphakia in Humans

5 Jul 2006

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 16826526
DOI: 10.1086/505654

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Related research

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Research trail→

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Homozygous Nonsense Mutation in the FOXE3 Gene as a Cause of Congenital Primary Aphakia in HumansPMID 16826526Read ↗

Lack of FOXE3 coding mutation in a case of congenital aphakia.Semantic proximity Read ↗

Foxe view of lens development and disease.Semantic proximity Read ↗

FOXE3 mutations: genotype-phenotype correlations.Semantic proximity Read ↗

Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders.Semantic proximity Read ↗

FOXE3 plays a significant role in autosomal recessive microphthalmia.Semantic proximity Read ↗

A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family.Semantic proximity Read ↗

Identification of OPN3 as associated with non-syndromic oligodontia in a Japanese population.Semantic proximity Read ↗

Homozygous nonsense mutation in HOXD13 underlies synpolydactyly with a cleft.Semantic proximity Read ↗

A Human Homeotic Transformation Resulting from Mutations in PLCB4 and GNAI3 Causes Auriculocondylar SyndromeSemantic proximity Read ↗

A Human Homeotic Transformation Resulting from Mutations in PLCB4 and GNAI3 Causes Auriculocondylar SyndromeSemantic proximity Read ↗

Sclerocornea-Microphthalmia-Aphakia Complex: Description of Two Additional Cases Associated With Novel FOXE3 Mutations and Review of the Literature.Semantic proximity Read ↗

Congenital Ichthyosis and Recurrent Eczema Associated with a Novel ALOXE3 Mutation.Semantic proximity Read ↗

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