1. A Mosaic Mutation in the LAMA2 Gene in a Case of Merosin-deficient Congenital Muscular Dystrophy
    P. A. Chausova et al, 2021, Frontiers in Genetics CrossRef
  2. Merosin-deficient congenital muscular dystrophy type 1a: detection of LAMA2 variants in Vietnamese patients
    Van Khanh Tran et al, 2023, Frontiers in Genetics CrossRef
  3. Whole Exome Sequencing as a Diagnostic Tool for Unidentified Muscular Dystrophy in a Vietnamese Family
    Ngoc-Lan Nguyen et al, 2020, Diagnostics CrossRef
  4. Identification of a novel pathogenic COL4A3 gene mutation in a Chinese family with autosomal dominant Alport syndrome: A case report
    Da-An Nie et al, 2021, Biomedical Reports CrossRef