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Updated: Oct 12, 2025

06:41
In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
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Localized autosomal recessive epidermolysis bullosa simplex arising from a novel homozygous frameshift mutation in
D Wen1,2, D L Balacco1, A Bardhan1,2
1Institute of Clinical Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Clinical and Experimental Dermatology
|November 22, 2021
Abstract
No abstract available in PubMed .
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