Related Experiment Video
Updated: Jul 2, 2026

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
A novel GJB6 missense mutation in hidrotic ectodermal dysplasia 2 (Clouston syndrome) broadens its genotypic basis
H N Baris1, A Zlotogorski, G Peretz-Amit
1The Raphael Recanati Genetic Institute, Rabin Medical Center, Beilinson Hospital, Petah Tikva 49100, Israel. barish@clalit.org.il
No abstract available in PubMed .
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