Genotype–Phenotype Correlation in Chinese Patients with Dystrophic Epidermolysis Bullosa Pruriginosa
Author:
Publisher
Medical Journals Sweden AB
Subject
Dermatology,General Medicine
Cited by 17 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. Missense Variant c.3301C>T (p.R1101W) in von Willebrand Factor A Sequence in a Patient with Recessive Dystrophic Epidermolysis Bullosa Pruriginosa with Compound Heterozygous COL7A1 Variants;Annals of Dermatology;2023
2. Complex genetic models in dystrophic epidermolysis bullosa families with marked intra‐familial phenotypic heterogeneity;Journal of the European Academy of Dermatology and Venereology;2022-02-28
3. Availability of mRNA Obtained from Peripheral Blood Mononuclear Cells for Testing Mutation Consequences in Dystrophic Epidermolysis Bullosa;International Journal of Molecular Sciences;2021-12-13
4. Dystrophic epidermolysis bullosa pruriginosa: a new case series of a rare phenotype unveils skewed Th2 immunity;Journal of the European Academy of Dermatology and Venereology;2021-10-15
5. Epidermolysis Bullosa in Chinese Patients: Genetic Analysis and Mutation Landscape in 57 Pedigrees and Sporadic Cases;Acta Dermato Venereologica;2021
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