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Volumn 9, Issue 4, 2003, Pages 16-19

Erythrokeratodermia variabilis

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANAMNESIS; CASE REPORT; CLINICAL FEATURE; CONFERENCE PAPER; ERYTHROKERATODERMA FIGURATA VARIABILIS; FEMALE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; KERATODERMA; LABORATORY TEST; SKIN DISEASE;

EID: 3042562290     PISSN: 10872108     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper
Times cited : (5)

References (4)
  • 1
    • 0029558383 scopus 로고
    • Erythrokeratodermia variabilis present at birth: Case report and review of the literature
    • Hendrix JD Jr, Greer KE. Erythrokeratodermia variabilis present at birth: case report and review of the literature. Pediatr Dermatol 1995;12:351.
    • (1995) Pediatr Dermatol , vol.12 , pp. 351
    • Hendrix Jr., J.D.1    Greer, K.E.2
  • 2
    • 0031796918 scopus 로고    scopus 로고
    • Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis
    • Richard G, et al. Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis. Nature Genet 1998;20:366.
    • (1998) Nature Genet , vol.20 , pp. 366
    • Richard, G.1
  • 3
    • 0343291147 scopus 로고    scopus 로고
    • Clinical heterogeneity in EKV
    • Richard G, et al. Clinical heterogeneity in EKV. J Invest Dermatol 1998;110:616.
    • (1998) J Invest Dermatol , vol.110 , pp. 616
    • Richard, G.1
  • 4
    • 0034073333 scopus 로고    scopus 로고
    • The spectrum of mutations in erythrokeratodermias-novel and de novo mutations in GJB3
    • Richard G, et al. The spectrum of mutations in erythrokeratodermias-novel and de novo mutations in GJB3. Hum Genet 2000;106:321.
    • (2000) Hum Genet , vol.106 , pp. 321
    • Richard, G.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.