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Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies

Authors:	Tahir N Khan Kamal Khan Azita Sadeghpour Hannah Reynolds Yezmin Perilla Marie T McDonald William B Gallentine Shahid M Baig

Institution:	1. Center for Human Disease Modeling, Duke University, Durham, NC 27701, USA;2. Human Molecular Genetics Laboratory, Health Biotechnology Division, National Institute for Biotechnology and Genetic Engineering, Faisalabad, Pakistan;3. Furman University, Greenville, SC 29613, USA;4. Department of Pediatrics, Division of Medical Genetics, Duke University Medical Center, Durham, NC 27710, USA;5. Department of Pediatrics, Division of Pediatric Neurology, Duke University Medical Center, Durham, NC 27710, USA

Abstract:

Keywords:	chromosome condensation microcephaly NPHP1 renal cyst zebrafish genetic interaction NCAPH2 NCAPD3 micronuclei cell cycle delay
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