Related Experiment Video
Updated: Apr 23, 2026

06:41
In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
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A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype
M Callea1, P Nieminen2, C E Willoughby3
1Institute for Maternal and Child Health - IRCCS 'Burlo Garofolo', Trieste, Italy.
Abstract
No abstract available in PubMed .
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