Skip to Main Content

Paper Details

Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
Nat Genet
85
2020
CTNNB1, Cerebral palsy, Drosophila, FBXO31, RHOB, RHOB mutation, Rho, Rho GTPase, TUBA1A, cerebral palsy, cyclin, neuritogenesis genes, neurodevelopmental disorder
Author NameAffiliation
Shozeb HaiderDepartment of Pharmaceutical and Biological Chemistry, UCL School of Pharmacy
Hongyu ZhaoYale School of Public Health
Christopher CastaldiYale Center for Genome Analysis, Yale University
Irina R TikhonovaYale Center for Genome Analysis, Yale University
Francesc L??pez-Gir??ldezYale Center for Genome Analysis, Yale University
Megan T Cho
Julie S CohenDivision of Neurogenetics and Hugo W. Moser Research Institute, Kennedy Krieger Institute
Angela E LinMassGeneral Hospital for Children
Timothy FeymaGillette Children's Hospital
Shrikant ManeYale Center for Genome Analysis, Yale University
Kaya BilguvarYale University School of Medicine
Kaya BilguvarYale Center for Genome Analysis, Yale University
Richard P LiftonYale University School of Medicine
Richard P LiftonRockefeller University
Richard P LiftonYale University School of Medicine
Richard P LiftonRockefeller University
  • 1 - 16

Datasets

Release 1.2