Differences in recurrent COL7A1 mutations in dystrophic epidermolysis bullosa: ethnic-specific and worldwide recurrent mutations
Author:
Publisher
Springer Science and Business Media LLC
Subject
Dermatology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00403-003-0444-1.pdf
Cited by 35 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. Functional genotype-phenotype associations in recessive dystrophic epidermolysis bullosa;Journal of the American Academy of Dermatology;2024-09
2. Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis;Dermatology and Therapy;2024-08-07
3. Increased healthcare burden and comorbidity risks of pediatric patients with dystrophic epidermolysis bullosa: Analysis of Nationwide Emergency Department Sample 2015–2019;Pediatric Dermatology;2024-07-25
4. Epidermolysis Bullosa: Two rare case reports of COL7A1 and EBS-GEN SEV KRT14 variants with review of literature;BMC Pediatrics;2024-04-05
5. Cytosine Deaminase Base Editing to Restore COL7A1 in Dystrophic Epidermolysis Bullosa Human: Murine Skin Model;JID Innovations;2023-05
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