@misc{indiciae6d87574305b8,
  title = {Specific OCRL1 patient mutations differentially impact Lowe Syndrome cellular phenotypes},
  author = {Ramadesikan, S. and Skiba, L. and Lee, J. and Madhivanan, K. and Sarkar, D. and De La Fuente, A. and Hanna, C. B. and Hazbun, T. and Kihara, D. and Aguilar, R. C.},
  year = {2020},
  doi = {10.1101/2020.08.04.236612},
  url = {https://www.biorxiv.org/content/10.1101/2020.08.04.236612v1},
  note = {Source identifier: 10.1101/2020.08.04.236612}
}