Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth.

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Title:	Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth.
Authors:	Jeanne M; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.; UMR 1253, iBrain, University of Tours, Inserm, Tours, France., Vuillaume ML; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.; UMR 1253, iBrain, University of Tours, Inserm, Tours, France., Ung DC; UMR 1253, iBrain, University of Tours, Inserm, Tours, France., Vancollie VE; Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, Hinxton, UK., Wagner C; Centre National de la Recherche Scientifique, UMR 7104, Illkirch, France.; Institut National de la Santé et de la Recherche Médicale (Inserm), U 1258, Illkirch, France.; Université de Strasbourg, Illkirch, France., Collins SC; Centre National de la Recherche Scientifique, UMR 7104, Illkirch, France.; Institut National de la Santé et de la Recherche Médicale (Inserm), U 1258, Illkirch, France.; Université de Strasbourg, Illkirch, France., Vonwill S; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France., Haye D; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France., Chelloug N; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France., Pfundt R; Department of Human Genetics, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands., Kummeling J; Department of Human Genetics, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands., Moizard MP; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France., Marouillat S; UMR 1253, iBrain, University of Tours, Inserm, Tours, France., Kleefstra T; Department of Human Genetics, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands., Yalcin B; Centre National de la Recherche Scientifique, UMR 7104, Illkirch, France.; Institut National de la Santé et de la Recherche Médicale (Inserm), U 1258, Illkirch, France.; Université de Strasbourg, Illkirch, France., Laumonnier F; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France. frederic.laumonnier@inserm.fr.; UMR 1253, iBrain, University of Tours, Inserm, Tours, France. frederic.laumonnier@inserm.fr., Toutain A; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.; UMR 1253, iBrain, University of Tours, Inserm, Tours, France.
Source:	Human genetics [Hum Genet] 2021 Jun; Vol. 140 (6), pp. 885-896. Date of Electronic Publication: 2021 Jan 08.
Publication Type:	Journal Article
Journal Info:	Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE
Database:	MEDLINE Ultimate

Description
ISSN:	1432-1203
DOI:	10.1007/s00439-020-02252-1