@misc{indiciaed4bd58b670b2,
  title = {Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1},
  author = {Wu, N. and Lin, M. and Liu, Z. and Liu, G. and Zhao, S. and Li, C. and Chen, W. and Akdemir, Z. C. and Lin, J. and Song, X. and Wang, S. and Xu, Q. and Zhao, Y. and Wang, L. and Zhang, Y. and Yan, Z. and Liu, S. and Liu, J. and Chen, Y. and Yang, X. and Sun, T. and Yang, X.-Z. and Niu, Y. and Li, X. and You, W. and Qiu, B. and Ding, C. and Liu, P. and Zhang, S. and Fonseca, C. and Posey, J. E. and Qiu, G. and Lupski, J. R. and Wu, Z. and Zhang, J.},
  year = {2019},
  doi = {10.1101/726646},
  url = {https://www.biorxiv.org/content/10.1101/726646v1},
  note = {Source identifier: 10.1101/726646}
}