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Article

A novel mutation in the helix termination motif of keratin K12 in a US family with Meesmann corneal dystrophy

1 Dec 1999

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Share to Corneal Surgery and Treatments
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 10612503
DOI: 10.1016/s0002-9394(99)00317-7

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Related research

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A novel mutation in the helix termination motif of keratin K12 in a US family with Meesmann corneal dystrophyPMID 10612503Read ↗

Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12.Semantic proximity Read ↗

Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene.Semantic proximity Read ↗

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Novel mutations in the helix termination motif of keratin 3 and keratin 12 in 2 Taiwanese families with Meesmann corneal dystrophy.Semantic proximity Read ↗

A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy.Semantic proximity Read ↗

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