Associated Papers
Merosin-deficient congenital muscular dystrophy type 1a: detection of LAMA2 variants in Vietnamese patients.
Tran VK et al.
Frontiers in Genetics, 2023
Whole Exome Sequencing as a Diagnostic Tool for Unidentified Muscular Dystrophy in a Vietnamese Family.
Nguyen NL et al.
Diagnostics (basel, Switzerland), 2020
A novel de novo variant of LAMA2 contributes to merosin deficient congenital muscular dystrophy type 1A: Case report.
Tran KT et al.
Biomedical Reports, 2020
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