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. 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