Bullous Dermolysis of the Newborn and Dystrophic Epidermolysis Bullosa Pruriginosa within the Same Family: Two Phenotypes Associated with a COL7A1 Mutation-Reference-Cited by-同舟云学术

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Bullous Dermolysis of the Newborn and Dystrophic Epidermolysis Bullosa Pruriginosa within the Same Family: Two Phenotypes Associated with a COL7A1 Mutation

Published:2011 Issue:6 Volume:91 Page:730-731
ISSN:0001-5555
Container-title:Acta Dermato Venereologica
language:en
Short-container-title:Acta Derm Venerol

Author:

Murase K,Kanoh H,Ishii N,Hashimoto T,Nakano H,Sawamura D,Seishima M

Publisher

Medical Journals Sweden AB

Subject

Dermatology,General Medicine

Cited by 14 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. Self‐improving dystrophic epidermolysis bullosa with a novel heterozygous missense variant in the COL7A1 gene in a Taiwanese family;Wound Repair and Regeneration;2024-02-28

2. Dystrophic epidermolysis bullosa: genotype-phenotype correlations;Vestnik dermatologii i venerologii;2023-10-16

3. A newborn with dystrophic epidermolysis bullosa, self-improving and mother with epidermolysis bullosa pruriginosa;Pediatrics & Neonatology;2023-09

4. COL7A1 G2287R mutation with two clinical phenotypes in the same family: Bullous dermolysis of the newborn and dystrophic epidermolysis bullosa pruriginosa;The Journal of Dermatology;2022-05-13

5. Novel COL7A1 mutation in a family with bullous dermolysis of the newborn: Phenotypic variability associated with a COL7A1 mutation within the same family;The Journal of Dermatology;2018-03-25

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