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Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly
Andrew DiStasio, Ashley Driver, Kristen Sund, Milene Donlin, Shabnam Pooya, Beth Kline-Fath, Kenneth M. Kaufman, Cynthia A. Prows, Elizabeth Schorry, Biplab DasGupta, Rolf Stottmann
doi: https://doi.org/10.1101/135236
Andrew DiStasio
1Division of Human Genetics, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229
Ashley Driver
1Division of Human Genetics, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229
Kristen Sund
1Division of Human Genetics, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229
Milene Donlin
1Division of Human Genetics, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229
Shabnam Pooya
2Division of Hematology and Oncology, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229
Beth Kline-Fath
3Department of Radiology, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229
Kenneth M. Kaufman
4Division of Rheumatology and Center for Autoimmune Genomics and Etiology, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229
Cynthia A. Prows
1Division of Human Genetics, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229
5Division of Patient Services, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229
Elizabeth Schorry
1Division of Human Genetics, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229
Biplab DasGupta
2Division of Hematology and Oncology, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229
Rolf Stottmann
1Division of Human Genetics, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229
6Division of Developmental Biology, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229
Article usage
Posted May 08, 2017.
Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly
Andrew DiStasio, Ashley Driver, Kristen Sund, Milene Donlin, Shabnam Pooya, Beth Kline-Fath, Kenneth M. Kaufman, Cynthia A. Prows, Elizabeth Schorry, Biplab DasGupta, Rolf Stottmann
bioRxiv 135236; doi: https://doi.org/10.1101/135236
Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly
Andrew DiStasio, Ashley Driver, Kristen Sund, Milene Donlin, Shabnam Pooya, Beth Kline-Fath, Kenneth M. Kaufman, Cynthia A. Prows, Elizabeth Schorry, Biplab DasGupta, Rolf Stottmann
bioRxiv 135236; doi: https://doi.org/10.1101/135236
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