No exonic mutations at GJB2, GJB3, GJB4, GJB6, ARS (Component B), and LOR genes responsible for a Chinese patient affected by progressive symmetric erythrokeratodermia with pseudoainhum-Reference-Cited by-同舟云学术

No exonic mutations at GJB2, GJB3, GJB4, GJB6, ARS (Component B), and LOR genes responsible for a Chinese patient affected by progressive symmetric erythrokeratodermia with pseudoainhum

Published:2014-06-25 Issue:9 Volume:53 Page:1111-1113
ISSN:0011-9059
Container-title:International Journal of Dermatology
language:en
Short-container-title:Int J Dermatol

Author:

Zhou Fusheng¹²³,Fu Hongyang¹²,Liu Linghua¹²,Cui Yong¹²,Zhang Zhengzhong⁴,Chang Ruixue¹²,Yue Zhen¹²,Yang Sen¹²³,Zhang Xuejun¹²

Affiliation:

1. Institute of Dermatology and Department of Dermatology at No. 1 Hospital; Anhui Medical University; Hefei Anhui China

2. Department of Dermatology and Venereology; Anhui Medical University; Hefei Anhui China

3. State Key Laboratory of Dermatology Incubation; Ministry of Science and Technology; Hefei Anhui China

4. Department of Dermatology; the Affiliated Hospital of North Sichuan Medical College; Nanchong China

Publisher

Wiley

Subject

Dermatology

Reference12 articles.

1. Is erythrokeratoderma one disorder? A clinical and ultrastructural study of two siblings;Macfarlane;Br J Dermatol,1991

2. The missense mutation G12D in connexin30.3 can cause both erythrokeratodermia variabilis of Mendes da Costa and progressive symmetric erythrokeratodermia of Gottron;Steensel;Am J Med Genet A,2009

3. Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis;Richard;Nat Genet,1998

4. Mutation in the gene for connexin 30.3 in a family with erythrokera- todermia variabilis;Macari;Am J Hum Genet,2000

5. [Pseudo-ainhum in Vohwinkel disease. Keratoma hereditarium mutilans];Bell;Hautarzt,1993

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3. Keratoderma;Atlas of Skin Disorders;2018