APA (7th ed.) Citation

HC, L., C, D., M, H., S, M., R, L., B, G., . . . JB, K. (2026). Ultra-rare variants in LAMA2 are risk factors for frontotemporal dementia and motor neuron disease. Human molecular genetics, 35(8), . https://doi.org/10.1093/hmg/ddag034

Chicago Style (17th ed.) Citation

HC, Lok, et al. "Ultra-rare Variants in LAMA2 Are Risk Factors for Frontotemporal Dementia and Motor Neuron Disease." Human Molecular Genetics 35, no. 8 (2026). https://doi.org/10.1093/hmg/ddag034.

MLA (9th ed.) Citation

HC, Lok, et al. "Ultra-rare Variants in LAMA2 Are Risk Factors for Frontotemporal Dementia and Motor Neuron Disease." Human Molecular Genetics, vol. 35, no. 8, 2026, https://doi.org/10.1093/hmg/ddag034.