Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12.
about
Identification of presumed pathogenic KRT3 and KRT12 gene mutations associated with Meesmann corneal dystrophy.Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophy.Familial Limbal Stem Cell Deficiency: Clinical, Cytological and Genetic Characterization.A corneal tulip? Assessing corneal opacities in Lisch corneal epithelial dystrophy
P2860
Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12.
description
2012 nî lūn-bûn
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2012年の論文
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2012年論文
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2012年論文
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2012年論文
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2012年論文
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2012年論文
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2012年论文
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2012年论文
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2012年论文
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name
Severe Meesmann's epithelial c ...... nitiation motif of keratin 12.
@ast
Severe Meesmann's epithelial c ...... nitiation motif of keratin 12.
@en
type
label
Severe Meesmann's epithelial c ...... nitiation motif of keratin 12.
@ast
Severe Meesmann's epithelial c ...... nitiation motif of keratin 12.
@en
prefLabel
Severe Meesmann's epithelial c ...... nitiation motif of keratin 12.
@ast
Severe Meesmann's epithelial c ...... nitiation motif of keratin 12.
@en
P2093
P2860
P356
P1433
P1476
Severe Meesmann's epithelial c ...... nitiation motif of keratin 12.
@en
P2093
P2860
P2888
P304
P356
10.1038/EYE.2012.261
P577
2012-12-07T00:00:00Z