A Novel COL7A1 Gene Mutation in an Iranian Individual Suffering Dystrophic Epidermolysis Bullosa
Author:
Publisher
Elsevier BV
Subject
Molecular Medicine,Pathology and Forensic Medicine
Reference20 articles.
1. Isolated nail dystrophy suggestive of dominant dystrophic epidermolysis bullosa;Tosti;Pediatr Dermatol,2003
2. Oral lesions in recessive dystrophic epidermolysis bullosa;Serrano-Martinez;Oral Dis,2003
3. Plectin deficiency results in muscular dystrophy with epidermolysis bullosa;Smith;Nat Genet,1996
4. Progress in epidermolysis bullosa: from eponyms to molecular genetics classification;Uitto;Clin Dermatol,2005
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Cited by 4 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. Investigation of Genetic Mutations in the Exon-intron Regions of the COL7A1 Gene in five Family Case Reports with Epidermolysis Bullosa in Khuzestan Province;Gene, Cell and Tissue;2023-02-01
2. Case report of two siblings with a novel homozygous mutation in COL7A1 leads to recessive dystrophic epidermolysis bullosa: which type?;Clinical Dysmorphology;2018-10
3. Genetics of Isolated Hereditary Nail Disorder;eLS;2017-09-15
4. Two Novel Mutations on Exon 8 and Intron 65 of COL7A1 Gene in Two Chinese Brothers Result in Recessive Dystrophic Epidermolysis Bullosa;PLoS ONE;2012-11-30
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