A case of erythrokeratoderma variabilis without mutations in connexin 31-Reference-Cited by-同舟云学术

A case of erythrokeratoderma variabilis without mutations in connexin 31

Published:2000-12 Issue:6 Volume:143 Page:1283-1287
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:British Journal of Dermatology

Author:

Ishida‐Yamamoto A.¹,Kelsell D.¹,Common J.¹,Houseman M.J.¹,Hashimoto M.¹,Shibaki H.¹,Asano K.¹,Takahashi H.¹,Hashimoto Y.¹,Senshu T.¹,Leigh I.M.¹,Iizuka H.¹

Affiliation:

1. Department of Dermatology, Asahikawa Medical College, Midorigaoka‐Higashi 2‐1‐1‐1, Asahikawa 078‐8510, Japan *The Centre for Cutaneous Research, St Bartholomew’s & the Royal London School of Medicine and Dentistry,  Queen Mary & Westfield College, London, U.K.  †Department of Cell Chemistry, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan ‡Molecular Medicine Unit, St. James’ University Hospital, Leeds, LS9 7TF, U.K.

Publisher

Wiley

Subject

Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1365-2133.2000.03902.x

Reference33 articles.

1. Erythro‐ et keratodermia variabilis in a mother and daughter;Mendes da Costa S.;Acta Derm Venereol (Stockh),1925

2. Érythème desquamatif en plaques, congenital et familial (genodermatose nouvelle?);Degos R;Bull Soc Fr Dermatol Syphilol,1947

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