A mutation (N177S) in the structurally conserved helix initiation peptide motif of keratin 5 causes a mild EBS phenotype (Q44893824)
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English | A mutation (N177S) in the structurally conserved helix initiation peptide motif of keratin 5 causes a mild EBS phenotype |
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A mutation (N177S) in the structurally conserved helix initiation peptide motif of keratin 5 causes a mild EBS phenotype (English)
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Liovic M
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Bowden PE
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Marks R
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Komel R
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1 May 2004
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13
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5
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332-334
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