Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability

Author:

Cogné Benjamin,Ehresmann Sophie,Beauregard-Lacroix Eliane,Rousseau Justine,Besnard Thomas,Garcia Thomas,Petrovski Slavé,Avni Shiri,McWalter Kirsty,Blackburn Patrick R.,Sanders Stephan J.,Uguen Kévin,Harris Jacqueline,Cohen Julie S.,Blyth Moira,Lehman Anna,Berg Jonathan,Li Mindy H.,Kini Usha,Joss Shelagh,von der Lippe Charlotte,Gordon Christopher T.,Humberson Jennifer B.,Robak Laurie,Scott Daryl A.,Sutton Vernon R.,Skraban Cara M.,Johnston Jennifer J.,Poduri Annapurna,Nordenskjöld Magnus,Shashi Vandana,Gerkes Erica H.,Bongers Ernie M.H.F.,Gilissen Christian,Zarate Yuri A.,Kvarnung Malin,Lally Kevin P.,Kulch Peggy A.,Daniels Brina,Hernandez-Garcia Andres,Stong Nicholas,McGaughran Julie,Retterer Kyle,Tveten Kristian,Sullivan Jennifer,Geisheker Madeleine R.,Stray-Pedersen Asbjorg,Tarpinian Jennifer M.,Klee Eric W.,Sapp Julie C.,Zyskind Jacob,Holla Øystein L.,Bedoukian Emma,Filippini Francesca,Guimier Anne,Picard Arnaud,Busk Øyvind L.,Punetha Jaya,Pfundt Rolph,Lindstrand Anna,Nordgren Ann,Kalb Fayth,Desai Megha,Ebanks Ashley Harmon,Jhangiani Shalini N.,Dewan Tammie,Coban Akdemir Zeynep H.,Telegrafi Aida,Zackai Elaine H.,Begtrup Amber,Song Xiaofei,Toutain Annick,Wentzensen Ingrid M.,Odent Sylvie,Bonneau Dominique,Latypova Xénia,Deb Wallid,Redon Sylvia,Bilan Frédéric,Legendre Marine,Troyer Caitlin,Whitlock Kerri,Caluseriu Oana,Murphree Marine I.,Pichurin Pavel N.,Agre Katherine,Gavrilova Ralitza,Rinne Tuula,Park Meredith,Shain Catherine,Heinzen Erin L.,Xiao Rui,Amiel Jeanne,Lyonnet Stanislas,Isidor Bertrand,Biesecker Leslie G.,Lowenstein Dan,Posey Jennifer E.,Denommé-Pichon Anne-Sophie,Férec Claude,Yang Xiang-Jiao,Rosenfeld Jill A.,Gilbert-Dussardier Brigitte,Audebert-Bellanger Séverine,Redon Richard,Stessman Holly A.F.,Nellaker Christoffer,Yang Yaping,Lupski James R.,Goldstein David B.,Eichler Evan E.,Bolduc Francois,Bézieau Stéphane,Küry Sébastien,Campeau Philippe M.

Funder

French Ministry of Health

Health Regional Agency from Poitou-Charentes

HUGODIMS

National Institute of Neurological Disorders and Stroke

The Epilepsy Phenome/Genome Project

Epi4K

National Institutes of Health/Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Human Genome Research Institute

National Heart, Lung, and Blood Institute

NHGRI

Duke Genome Sequencing Clinic

intramural research program of the NHGRI

US National Institute of Mental Health

Kids Brain Health Network

Dart NeuroScience

Mining for Miracles

British Columbia Children’s Hospital Foundation

Genome British Columbia

CIHR

FRSQ

Mayo Clinic Center for Individualized Medicine

CIM Investigative and Functional Genomics Program

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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