Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome

Author:

Tessadori Federico,Duran Karen,Knapp Karen,Fellner Matthias,Smithson Sarah,Beleza Meireles Ana,Elting Mariet W.,Waisfisz Quinten,O’Donnell-Luria Anne,Nowak Catherine,Douglas Jessica,Ronan Anne,Brunet Theresa,Kotzaeridou Urania,Svihovec Shayna,Saenz Margarita S.,Thiffault Isabelle,Del Viso Florencia,Devine Patrick,Rego Shannon,Tenney Jessica,van Haeringen Arie,Ruivenkamp Claudia A.L.,Koene Saskia,Robertson Stephen P.,Deshpande Charulata,Pfundt Rolph,Verbeek Nienke,van de Kamp Jiddeke M.,Weiss Janneke M.M.,Ruiz Anna,Gabau Elisabeth,Banne Ehud,Pepler Alexander,Bottani Armand,Laurent Sacha,Guipponi Michel,Bijlsma Emilia,Bruel Ange-Line,Sorlin Arthur,Willis Mary,Powis Zoe,Smol Thomas,Vincent-Delorme Catherine,Baralle Diana,Colin Estelle,Revencu Nicole,Calpena Eduardo,Wilkie Andrew O.M.,Chopra Maya,Cormier-Daire Valerie,Keren Boris,Afenjar Alexandra,Niceta Marcello,Terracciano Alessandra,Specchio Nicola,Tartaglia Marco,Rio Marlene,Barcia Giulia,Rondeau Sophie,Colson Cindy,Bakkers Jeroen,Mace Peter D.,Bicknell Louise S.,van Haaften GijsORCID

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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