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Mutations in PURA cause profound neonatal hypotonia, seizures, and encephalopathy in 5q31.3 microdeletion syndrome

  • Seema R. Lalani
  • , Jing Zhang
  • , Christian P. Schaaf
  • , Chester W. Brown
  • , Pilar Magoulas
  • , Anne Chun Hui Tsai
  • , Areeg El-Gharbawy
  • , Klaas J. Wierenga
  • , Dennis Bartholomew
  • , Chin To Fong
  • , Tina Barbaro-Dieber
  • , Mary K. Kukolich
  • , Lindsay C. Burrage
  • , Elise Austin
  • , Kory Keller
  • , Matthew Pastore
  • , Fabio Fernandez
  • , Timothy Lotze
  • , Angus Wilfong
  • , Gabriela Purcarin
    • Wenmiao Zhu, William J. Craigen, Marianne McGuire, Mahim Jain, Erin Cooney, Mahshid Azamian, Matthew N. Bainbridge, Donna M. Muzny, Eric Boerwinkle, Richard E. Person, Zhiyv Niu, Christine M. Eng, James R. Lupski, Richard A. Gibbs, Arthur L. Beaudet, Yaping Yang, Meng C. Wang, Fan Xia

Research output: Contribution to journal › Article › peer-review

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Biochemistry, Genetics and Molecular Biology