Hastings, R., de Villiers, C. P., Hooper, C., Ormondroyd, L., Pagnamenta, A., Lise, S., Salatino, S., Knight, S. J., Taylor, J. C., Thomson, K. L., Arnold, L., Chatziefthimiou, S. D., Konarev, P. V., Wilmanns, M., Ehler, E., Ghisleni, A., Gautel, M., Blair, E., Watkins, H., & Gehmlich, K. (2016). combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction. Circulation, 9, . http://access.bl.uk/ark:/81055/vdc_100041981300.0x000008