Ectodermal dysplasia‐skin fragility syndrome: two new cases with a novel missense mutation-Reference-Cited by-同舟云学术

Ectodermal dysplasia‐skin fragility syndrome: two new cases with a novel missense mutation

Published:2020-10-30 Issue:4 Volume:19 Page:595-597
ISSN:1610-0379
Container-title:JDDG: Journal der Deutschen Dermatologischen Gesellschaft
language:en
Short-container-title:JDDG: Journal der Deutschen Dermatologischen Gesellschaft

Author:

Cuenca‐Barrales Carlos¹,Monserrat‐García María Teresa²,Domínguez‐Cruz Javier Jesús²,Suñol‐Capella Mariona³,Zulueta‐Dorado Teresa⁴,Fernández Raquel⁵,Mascaró José Manuel⁶,Vicente Asunción⁷,Bernabéu‐Wittel José²

Affiliation:

1. Department of Dermatology Hospital Universitario San Cecilio Granada Spain

2. Pediatric Dermatology Unit Hospital Universitario Virgen del Rocío Sevilla Spain

3. Department of Pathology Hospital Sant Joan de Déu Barcelona Spain

4. Department of Pathology Hospital Universitario Virgen del Rocío Sevilla Spain

5. Department of Genetics Hospital Universitario Virgen del Rocío Sevilla Spain

6. Department of Dermatology Hospital Clínic de Barcelona Barcelona Spain

7. Department of Dermatology Hospital Sant Joan de Déu Barcelona Spain

Publisher

Wiley

Subject

Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ddg.14315

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Ectodermal dysplasia-skin fragility syndrome – identification of a novel plakophilin1 (PKP1) gene variant through whole exome sequencing;Indian Journal of Dermatology, Venereology and Leprology;2024-03-02

2. McGrath Syndrome;Genetic Syndromes;2023