Related Experiment Video
Updated: Mar 18, 2026

06:41
In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
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Syndromic inherited poikiloderma due to a de novo mutation in FAM111B
T Takeichi1,2, A Nanda3, H-S Yang4
1St John's Institute of Dermatology, King's College London, Guy's Hospital, London, U.K.
The British Journal of Dermatology
|July 14, 2016
Abstract
No abstract available in PubMed .
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