YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction

Author:

Gabriele Michele,Vulto-van Silfhout Anneke T.,Germain Pierre-Luc,Vitriolo Alessandro,Kumar Raman,Douglas Evelyn,Haan Eric,Kosaki Kenjiro,Takenouchi Toshiki,Rauch Anita,Steindl Katharina,Frengen Eirik,Misceo Doriana,Pedurupillay Christeen Ramane J.,Stromme Petter,Rosenfeld Jill A.,Shao Yunru,Craigen William J.,Schaaf Christian P.,Rodriguez-Buritica David,Farach Laura,Friedman Jennifer,Thulin Perla,McLean Scott D.,Nugent Kimberly M.,Morton Jenny,Nicholl Jillian,Andrieux Joris,Stray-Pedersen Asbjørg,Chambon Pascal,Patrier Sophie,Lynch Sally A.,Kjaergaard Susanne,Tørring Pernille M.,Brasch-Andersen Charlotte,Ronan Anne,van Haeringen Arie,Anderson Peter J.,Powis Zöe,Brunner Han G.,Pfundt Rolph,Schuurs-Hoeijmakers Janneke H.M.,van Bon Bregje W.M.,Lelieveld Stefan,Gilissen Christian,Nillesen Willy M.,Vissers Lisenka E.L.M.,Gecz Jozef,Koolen David A.,Testa Giuseppe,de Vries Bert B.A.

Funder

European Commission

European Research Council

Telethon Foundation

Associazione Italiana per la Ricerca sul Cancro

Regione Lombardia

Umberto Veronesi Foundation

Italian Ministry of Health

Japan Agency for Medical Research and Development

Australian National Health and Medical Research Council

Dutch Organization for Health Research and Development

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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