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Updated: Aug 14, 2025

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
The family reported to have X-linked Dyggve-Melchior-Clausen syndrome instead has X-linked SEDT caused by a novel
Juan J Yunis1,2,3, Luz K Yunis1,3
1Grupo Patología Molecular, Facultad de Medicina e Instituto de Genética Universidad Nacional de Colombia, Bogotá, Colombia.
Abstract:
The family reported to have X-linked Dyggve-Melchior-Clausen syndrome instead has X-linked SEDT caused by a novel TRAPPC2 frameshift variant.
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