Associated Papers
Unraveling genetic etiologies in complex pediatric neurological diseases: A genetic investigation using whole exome sequencing.
Gaouzi Z et al.
Plos One, 2025
The role of the dystrophin glycoprotein complex in muscle cell mechanotransduction.
Wilson DGS et al.
Communications Biology, 2022
Case Report: A Boy From a Consanguineous Family Diagnosed With Congenital Muscular Dystrophy Caused by Integrin Alpha 7 (ITGA7) Mutation.
Xia W et al.
Frontiers in Genetics, 2021
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