Khan et al., 2019 - Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies. American journal of human genetics   104:94-111 Full text @ Am. J. Hum. Genet.
Morpholino List (2 Records)
Target Reagent
ncapg2 MO1-ncapg2
nphp1 MO3-nphp1