Mutations in ARMC9 , which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish

Author:

Van De Weghe Julie C.,Rusterholz Tamara D.S.,Latour Brooke,Grout Megan E.,Aldinger Kimberly A.,Shaheen Ranad,Dempsey Jennifer C.,Maddirevula Sateesh,Cheng Yong-Han H.,Phelps Ian G.,Gesemann Matthias,Goel Himanshu,Birk Ohad S.,Alanzi Talal,Rawashdeh Rifaat,Khan Arif O.,Bamshad Michael J.,Nickerson Deborah A.,Neuhauss Stephan C.F.,Dobyns William B.,Alkuraya Fowzan S.,Roepman Ronald,Bachmann-Gagescu Ruxandra,Doherty Dan

Funder

NIH Eunice Kennedy Shriver National Institute of Child Health and Human Development

NIH National Institute of Neurological Diseases and Stroke

Swiss National Science Foundation

Netherlands Organization for Scientific Research

King Salman Center for Disability Research

Dandy-Walker Alliance

NIH National Human Genome Research Institute

Saudi Human Genome Program

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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