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Volumn 159, Issue 6, 2008, Pages 1370-1372

Weber-Cockayne type of epidermolysis bullosa simplex associated with a novel mutation in keratin 5 and amyloid deposits

Author keywords

Amyloid; Epidermolysis bullosa simplex; Keratin 5; Novel mutation; Weber Cockayne

Indexed keywords

AMYLOID; CYTOKERATIN 14; CYTOKERATIN 5; DNA;

EID: 56549109174     PISSN: 00070963     EISSN: 13652133     Source Type: Journal    
DOI: 10.1111/j.1365-2133.2008.08801.x     Document Type: Article
Times cited : (3)

References (6)
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  • 2
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    • The Human Intermediate Filament Database: Comprehensive information on a gene family involved in many human diseases
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  • 3
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    • Epidermolysis bullosa simplex in Israel: Clinical and genetic features
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    • (2003) Arch Dermatol , vol.139 , pp. 498-505
    • Ciubotaru, D.1    Bergman, R.2    Baty, D.3
  • 4
    • 0022244963 scopus 로고
    • Epidermolysis bullosa of the Weber-Cockayne type with macular amyloidosis
    • Kantor GR, Kasick JM, Bergfeld WF et al. Epidermolysis bullosa of the Weber-Cockayne type with macular amyloidosis. Cleve Clin Q 1985 52 : 425 8.
    • (1985) Cleve Clin Q , vol.52 , pp. 425-8
    • Kantor, G.R.1    Kasick, J.M.2    Bergfeld, W.F.3
  • 6
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    • Macular amyloidosis: Etiological factors
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    • Eswaramoorthy, V.1    Kaur, I.2    Das, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.