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epidermolysis bullosa simplex, recessive
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KRT14
Missing links: Weber-Cockayne keratin mutations implicate the L12 linker domain in effective cytoskeleton function
A novel three-nucleotide deletion in the helix 2B region of keratin 14 in epidermolysis bullosa simplex: delta E375
A human keratin 14 "knockout": the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament protein
KRT5
Making a connection: direct binding between keratin intermediate filaments and desmosomal proteins
Epidermolysis bullosa simplex: a keratin 5 mutation is a fully dominant allele in epidermal cytoskeleton function
A common keratin 5 gene mutation in epidermolysis bullosa simplex--Weber-Cockayne
Allelic variations of human keratins K4 and K5 provide polymorphic markers within the type II keratin gene cluster on chromosome 12
DST
Isolation of complementary DNA for bullous pemphigoid antigen by use of patients' autoantibodies
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