Cite

    Cumming, S., Hamilton, M., Robb, Y., Gregory, H., McWilliam, C., Cooper, A., Adam, B., McGhie, J., Hamilton, G., Herzyk, P., Tschannen, M., Worthey, E., Petty, R., Ballantyne, B., Warner, J., Farrugia, M., Longman, C., & Monckton, D. (2018). de novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1. European journal of human genetics, 26, 1635–1647. http://access.bl.uk/ark:/81055/vdc_100084799062.0x000180