Clinical heterogeneity in recessive epidermolysis bullosa due to mutations in the keratin 14 gene, KRT14.
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Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta.Blistering disease: insight from the hemidesmosome and other components of the dermal-epidermal junction.Epidermal growth factor-induced modulation of cytokeratin expression levels influences the morphological phenotype of head and neck squamous cell carcinoma cells.Autosomal recessive epidermolysis bullosa simplex: report of three cases from India.Autosomal recessive epidermolysis bullosa simplex due to KRT14 mutation: two large Palestinian families and literature review.Immunofluorescence mapping in inherited epidermolysis bullosa: a study of 86 cases from India.Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplex.
P2860
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P2860
Clinical heterogeneity in recessive epidermolysis bullosa due to mutations in the keratin 14 gene, KRT14.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 16 August 2008
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Clinical heterogeneity in rece ...... in the keratin 14 gene, KRT14.
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Clinical heterogeneity in rece ...... in the keratin 14 gene, KRT14.
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type
label
Clinical heterogeneity in rece ...... in the keratin 14 gene, KRT14.
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Clinical heterogeneity in rece ...... in the keratin 14 gene, KRT14.
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prefLabel
Clinical heterogeneity in rece ...... in the keratin 14 gene, KRT14.
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Clinical heterogeneity in rece ...... in the keratin 14 gene, KRT14.
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P2093
P1476
Clinical heterogeneity in rece ...... in the keratin 14 gene, KRT14
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P2093
D F Murrell
E Yiasemides
N Trisnowati
S Klingberg
P304
P356
10.1111/J.1365-2230.2008.02858.X
P50
P577
2008-08-16T00:00:00Z