A novel pathogenic mutation in the COL7A1 gene resulting in mild autosomal dominant bullous dermolysis of the newborn-Reference-Cited by-同舟云学术

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A novel pathogenic mutation in the COL7A1 gene resulting in mild autosomal dominant bullous dermolysis of the newborn

Published:2020-06-16 Issue:5 Volume:37 Page:955-957
ISSN:0736-8046
Container-title:Pediatric Dermatology
language:en
Short-container-title:Pediatr Dermatol

Author:

Lor Michael¹^ORCID,Liu Michael¹,Kuklinski Lawrence F.¹,Hogeling Marcia¹

Affiliation:

1. Division of Dermatology Department of Medicine David Geffen School of Medicine University of California Los Angeles CA USA

Publisher

Wiley

Subject

Dermatology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/pde.14239

Reference6 articles.

1. Inherited epidermolysis bullosa

2. Inherited epidermolysis bullosa: Updated recommendations on diagnosis and classification

3. The international dystrophic epidermolysis bullosa patient registry: An online database of dystrophic epidermolysis bullosa patients and their COL7A1 mutations

4. Frequent occurrence of aplasia cutis congenita in bullous dermolysis of the newborn;Diociaiuti A;Acta Derm Venereol,2016

5. Novel COL7A1 mutation in a family with bullous dermolysis of the newborn: Phenotypic variability associated with a COL7A1 mutation within the same family

Cited by 1 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. Congenital absence of the skin secondary to the self-improving subtype of dystrophic epidermolysis bullosa with recurrent lesions throughout early childhood;JAAD Case Reports;2021-01

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