Related Experiment Video
Updated: Sep 15, 2025

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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Cerebrotendinous Xanthomatosis With a Heterozygous Frameshift Mutation Involving CYP27A1(C.526del)
Ajitesh Roy1, Sounak Kumar Roy2, Soumyadip Das2
1Department of Endocrinology, Vivekananda Institute of Medical Sciences, Kolkata, West Bengal 700026, India.
JCEM Case Reports
|July 17, 2025
Abstract
No abstract available in PubMed .
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