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Updated: Jul 6, 2026

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
Two non-contiguous duplications in the DMD gene in a Spanish family
M Fenollar-Cortés1, J Gallego-Merlo, M J Trujillo-Tiebas
1Servicio de Análisis Clínicos, Hospital Clínico San Carlos, Madrid, Spain. mfenollar.hcsc@salud.madrid.org
Abstract:
DMD and BMD are X-linked myopathy diseases in most cases caused by intragenic deletions, but duplications also appear in a significant number of cases. We present a complex duplication pattern detected by MLPA, a recently formulated method applied here to amplify the 79 exons of the DMD gene. We found a double-duplication in two DMD-affected brothers and in their carrier mother, which consist of two non-contiguous duplications encompassing exons 2 to 7 and exons 50 to 55. Different models are presented to explain formation of this genetic variant.
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