1. Oliveira, Jorge, Gruber, Angela, Cardoso, Márcio, Santos, Rosário, Sousa, Mário. 2018. LAMA2 gene mutation update: Toward a more comprehensive picture of the laminin-α2 variome and its related phenotypes. In Human mutation, 39, 1314-1337. doi:10.1002/humu.23599. https://pubmed.ncbi.nlm.nih.gov/30055037/
2. Liang, Jinghui, Li, Haixia, Han, Jingyi, Lv, Bin, Tian, Hui. 2020. Mex3a interacts with LAMA2 to promote lung adenocarcinoma metastasis via PI3K/AKT pathway. In Cell death & disease, 11, 614. doi:10.1038/s41419-020-02858-3. https://pubmed.ncbi.nlm.nih.gov/32792503/
3. Sarkozy, Anna, Foley, A Reghan, Zambon, Alberto A, Bönnemann, Carsten G, Muntoni, Francesco. 2020. LAMA2-Related Dystrophies: Clinical Phenotypes, Disease Biomarkers, and Clinical Trial Readiness. In Frontiers in molecular neuroscience, 13, 123. doi:10.3389/fnmol.2020.00123. https://pubmed.ncbi.nlm.nih.gov/32848593/
4. Li, Lei, Kang, Jia, Zhang, Ye, Chen, Juan, Zhu, Lan. 2019. LAMC1, LAMA2 and LAMA3 gene polymorphisms and the risk for severe pelvic organ prolapse. In Science bulletin, 64, 466-468. doi:10.1016/j.scib.2019.02.007. https://pubmed.ncbi.nlm.nih.gov/36659797/
5. Veyssiere, Maëva, Rodriguez Ordonez, Maria Del Pilar, Chalabi, Smahane, Petit-Teixeira, Elisabeth, Chaudru, Valérie. 2024. MYLK*FLNB and DOCK1*LAMA2 gene-gene interactions associated with rheumatoid arthritis in the focal adhesion pathway. In Frontiers in genetics, 15, 1375036. doi:10.3389/fgene.2024.1375036. https://pubmed.ncbi.nlm.nih.gov/38803542/
6. Yurchenco, Peter D, McKee, Karen K. 2019. Linker Protein Repair of LAMA2 Dystrophic Neuromuscular Basement Membranes. In Frontiers in molecular neuroscience, 12, 305. doi:10.3389/fnmol.2019.00305. https://pubmed.ncbi.nlm.nih.gov/31920536/
7. Rui, Qiang, Tan, Jing, Jin, Jing, Zhou, Yaping, Chen, Junqing. 2022. Establishment of a PBMC-derived induced pluripotent stem cell (NJUCMi001-A) from a patient with LAMA2-related congenital muscular dystrophy (MDC1A) carrying frameshift deletion c.3367delA in LAMA2 gene. In Stem cell research, 65, 102957. doi:10.1016/j.scr.2022.102957. https://pubmed.ncbi.nlm.nih.gov/36334577/
8. Bouman, Karlijn, Gubbels, Madelief, van den Heuvel, Frederik M A, Udink Ten Cate, Floris E A, Voermans, Nicol C. 2022. Cardiac involvement in two rare neuromuscular diseases: LAMA2-related muscular dystrophy and SELENON-related myopathy. In Neuromuscular disorders : NMD, 32, 635-642. doi:10.1016/j.nmd.2022.06.004. https://pubmed.ncbi.nlm.nih.gov/35868898/
智鼠故事 
