A novel mutation of keratin 5 in epidermolysis bullosa simplex with migratory circinate erythema-Reference-Cited by-同舟云学术

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A novel mutation of keratin 5 in epidermolysis bullosa simplex with migratory circinate erythema

Published:2020-03 Issue:2 Volume:37 Page:358-361
ISSN:0736-8046
Container-title:Pediatric Dermatology
language:en
Short-container-title:Pediatr Dermatol

Author:

Yalici‐Armagan Basak¹^ORCID,Kabacam Serkan²,Taskiran Zihni Ekim³,Gököz Özay⁴,Utine Gülen Eda⁵,Ersoy‐Evans Sibel¹

Affiliation:

1. Department of Dermatology and Venereology Faculty of Medicine Hacettepe University Ankara Turkey

2. Department of Medical Genetics Faculty of Medicine, Molecular Biologist Hacettepe University Ankara Turkey

3. Department of Medical Genetics Faculty of Medicine Hacettepe University Ankara Turkey

4. Department of Pathology Faculty of Medicine Hacettepe University Ankara Turkey

5. Department of Pediatric Genetics Faculty of Medicine Hacettepe University Ankara Turkey

Publisher

Wiley

Subject

Dermatology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/pde.14087

Reference10 articles.

1. Mutations in KRT5 and KRT14 cause epidermolysis bullosa simplex in 75% of the patients

2. A Usual Frameshift and Delayed Termination Codon Mutation in Keratin 5 Causes a Novel Type of Epidermolysis Bullosa Simplex with Migratory Circinate Erythema

3. Distinct phenotype of epidermolysis bullosa simplex with infantile migratory circinate erythema due to frameshift mutations in the V2 domain of KRT5

4. Mutational analysis on 16 Japanese population cases with epidermolysis bullosa simplex

5. T-lymphocytes are Directly Involved in the Clinical Expression of Migratory Circinate Erythema in Epidermolysis Bullosa Simplex Patients

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