1. Novel Gene LAMA2 Mutation and Exonic Deletion Underline Merosin-Deficient Congenital Muscular Dystrophy 1A in a Chinese Family
    Lili Liang et al, 2017, Iran J Pediatr CrossRef
  2. Identification of Two Novel LAMA2 Mutations in a Chinese Patient with Congenital Muscular Dystrophy
    Jing Zhou et al, 2018, Front. Genet. CrossRef
  3. Clinical and molecular-genetic profiles of patients with morphological indications of congenital multicore myopathy
    AA Kozina et al, 2019, BRSMU CrossRef
  4. A novel early onset phenotype in a zebrafish model of merosin deficient congenital muscular dystrophy
    Sarah J. Smith et al, 2017, PLoS ONE CrossRef
  5. Whole Exome Sequencing as a Diagnostic Tool for Unidentified Muscular Dystrophy in a Vietnamese Family
    Ngoc-Lan Nguyen et al, 2020, Diagnostics CrossRef
  6. Advances in CRISPR/Cas9 Genome Editing for the Treatment of Muscular Dystrophies
    Sina Fatehi et al, 2023, Human Gene Therapy CrossRef
  7. The congenital muscular dystrophies
    Haluk Topaloğlu et al, 2023, Annals of the Child Neurology Society CrossRef
  8. Myelin abnormalities in merosin‐deficient congenital muscular dystrophy
    Yoshihiko Saito et al, 2024, Muscle and Nerve CrossRef