Potential <scp>di‐genic</scp> contribution to guttate leukoderma as the predominant feature of epidermolysis bullosa simplex-Reference-Cited by-同舟云学术

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Potential di‐genic contribution to guttate leukoderma as the predominant feature of epidermolysis bullosa simplex

Published:2022-08-23 Issue:12 Volume:31 Page:1927-1931
ISSN:0906-6705
Container-title:Experimental Dermatology
language:en
Short-container-title:Experimental Dermatology

Author:

Koren Tamar¹,Zagairy Fadia¹,Tatour Yasmin²,Belhanes‐Peled Hila³,Khayat Morad²,Krausz Judit³,Danial‐Farran Nada²,Ziv Michael¹,Cohen‐Barak Eran¹⁴^ORCID

Affiliation:

1. Department of Dermatology “Emek” Medical Center Afula Israel

2. The Genetic Institute “Emek” Medical Center Afula Israel

3. The Institute of Tissue Diagnostics and Cancer Research Emek Medical Center Afula Israel

4. Bruce and Ruth Rappaport Faculty of Medicine Technion Haifa Israel

Publisher

Wiley

Subject

Dermatology,Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/exd.14661

Reference12 articles.

1. Inherited epidermolysis bullosa: New diagnostics and new clinical phenotypes

2. Germline Mutation in EXPH5 Implicates the Rab27B Effector Protein Slac2-b in Inherited Skin Fragility

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

4. Association of Epidermolysis Bullosa Simplex With Mottled Pigmentation andEXPH5Mutations

5. Autosomal recessive epidermolysis bullosa simplex due to EXPH5 mutation: neonatal diagnosis of the first Italian case and literature review

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. Epidermolysis bullosa simplex caused by a rare homozygous mutation in the EXPH5 gene;Clinical and Experimental Dermatology;2023-07-18

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