Novel splice mutation in CDSN gene causing type b peeling skin syndrome-Reference-Cited by-同舟云学术

Novel splice mutation in CDSN gene causing type b peeling skin syndrome

Published:2022-02-03 Issue:6 Volume:36 Page:
ISSN:0926-9959
Container-title:Journal of the European Academy of Dermatology and Venereology
language:en
Short-container-title:Acad Dermatol Venereol

Author:

Navarro‐Navarro I.¹^ORCID,Jiménez‐Gallo D.¹^ORCID,Varga‐Martínez R.²^ORCID,Villegas‐Romero I.¹^ORCID,Mora‐López F.²^ORCID,Linares‐Barrios M.¹^ORCID,Youssefian L.³^ORCID,Vahidnezhad H.³^ORCID,Uitto J.³^ORCID

Affiliation:

1. Unidad de Gestión Clínica de Dermatología Médico‐Quirúrgica y Venereología Hospital Universitario Puerta del Mar Cádiz Spain

2. Servicio de Inmunología Unidad de Gestión Clínica de Hematología Inmunología y Genética Hospital Universitario Puerta del Mar Cádiz España

3. Department of Dermatology and Cutaneous Biology Sidney Kimmel Medical College at Thomas Jefferson University Philadelphia PA USA

Publisher

Wiley

Subject

Infectious Diseases,Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jdv.17949

Reference10 articles.

1. Peeling Skin Disorders: A Paradigm for Skin Desquamation

2. Corneodesmosomes and corneodesmosin: from the stratum corneum cohesion to the pathophysiology of genodermatoses

3. Mutations in genes encoding desmosomal proteins: spectrum of cutaneous and extracutaneous abnormalities*

4. Loss of Corneodesmosin Leads to Severe Skin Barrier Defect, Pruritus, and Atopy: Unraveling the Peeling Skin Disease

5. Inflammatory Peeling Skin Syndrome Caused by a Mutation in CDSN Encoding Corneodesmosin

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