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Volumn 23, Issue 2, 2009, Pages 174-176

Identification of two recurrent mutations in keratin genes in three cases with pachyonychia congenita

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; CYTOKERATIN 16; LEUCINE; PROLINE;

EID: 58449088741     PISSN: 09269959     EISSN: 14683083     Source Type: Journal    
DOI: 10.1111/j.1468-3083.2008.02752.x     Document Type: Letter
Times cited : (5)

References (5)
  • 1
    • 0038326541 scopus 로고    scopus 로고
    • The molecular genetics of keratin disorders
    • Smith F. The molecular genetics of keratin disorders. Am J Clin Dermatol 2003 4 : 347 364.
    • (2003) Am J Clin Dermatol , vol.4 , pp. 347-364
    • Smith, F.1
  • 3
    • 0033381920 scopus 로고    scopus 로고
    • Novel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1
    • Smith FJD, Del Monaco M, Steijlen PM et al. Novel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1. Br J Dermatol 1999 141 : 1010 1016.
    • (1999) Br J Dermatol , vol.141 , pp. 1010-1016
    • Smith, F.J.D.1    Del Monaco, M.2    Steijlen, P.M.3
  • 5
    • 0026511054 scopus 로고
    • Do the ends justify the means? Proline mutations at the ends of the keratin coiled-coil rod segment are more disruptive than internal mutations
    • Letai A, Coulombe PA, Fuchs E. Do the ends justify the means? Proline mutations at the ends of the keratin coiled-coil rod segment are more disruptive than internal mutations. J Cell Biol 1992 116 : 1181 1195.
    • (1992) J Cell Biol , vol.116 , pp. 1181-1195
    • Letai, A.1    Coulombe, P.A.2    Fuchs, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.