ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder

Author:

Cuvertino Sara,Stuart Helen M.,Chandler Kate E.,Roberts Neil A.,Armstrong Ruth,Bernardini Laura,Bhaskar Sanjeev,Callewaert Bert,Clayton-Smith Jill,Davalillo Cristina Hernando,Deshpande Charu,Devriendt Koenraad,Digilio Maria C.,Dixit Abhijit,Edwards Matthew,Friedman Jan M.,Gonzalez-Meneses Antonio,Joss Shelagh,Kerr Bronwyn,Lampe Anne Katrin,Langlois Sylvie,Lennon Rachel,Loget Philippe,Ma David Y.T.,McGowan Ruth,Des Medt Maryse,O’Sullivan James,Odent Sylvie,Parker Michael J.,Pebrel-Richard Céline,Petit Florence,Stark Zornitza,Stockler-Ipsiroglu Sylvia,Tinschert Sigrid,Vasudevan Pradeep,Villa Olaya,White Susan M.,Zahir Farah R.,Woolf Adrian S.,Banka Siddharth

Funder

Newlife Foundation

Medical Research Council UK

Central Manchester University Hospitals NHS Foundation Trust

Kabuki Research Fund

Kidney Research UK

NIHR

Academy of Medical Sciences

Wellcome Trust

Health Innovation Challenge Fund

Wellcome Trust Sanger Institute

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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