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Updated: Nov 17, 2025

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
A novel GTPBP2 splicing mutation in two siblings affected with microcephaly, generalized muscular atrophy, and
Isa Abdi Rad1,2, Ali Vahabi2, Elinaz Akbariazar2
1Cellular and Molecular Research Center Urmia University of Medical Sciences Urmia Iran.
Abstract:
A novel splice site mutation in the GTPBP2 gene was identified by whole-exome sequencing in two siblings with microcephaly and progressive generalized muscular atrophy associated with hypotrichosis.
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