Characterization of Two Mouse <i>Chd7</i> Heterozygous Loss-of-Function Models Shows Dysgenesis of the Corpus Callosum and Previously Unreported Features of CHARGE Syndrome.

Collins, Stephan C; Vancollie, Valerie E; Mikhaleva, Anna; Wagner, Christel; Balz, Rebecca; Lelliott, Christopher J; Yalcin, Binnaz

Characterization of Two Mouse Chd7 Heterozygous Loss-of-Function Models Shows Dysgenesis of the Corpus Callosum and Previously Unreported Features of CHARGE Syndrome.

Collins, Stephan C; Vancollie, Valerie E; Mikhaleva, Anna; Wagner, Christel; Balz, Rebecca; Lelliott, Christopher J; Yalcin, Binnaz.

Affiliation

Collins SC; Inserm UMR1231, University of Burgundy Franche-Comté, 15 Boulevard Maréchal de Lattre de Tassigny, 21070 Dijon, France.
Vancollie VE; Wellcome Sanger Institute, Hinxton CB10 1SA, UK.
Mikhaleva A; Center for Integrative Genomics, University of Lausanne, 1015 Lausanne, Switzerland.
Wagner C; Institute of Genetics and Molecular and Cellular Biology, UMR7104, 67400 Illkirch, France.
Balz R; Center for Integrative Genomics, University of Lausanne, 1015 Lausanne, Switzerland.
Lelliott CJ; Wellcome Sanger Institute, Hinxton CB10 1SA, UK.
Yalcin B; Inserm UMR1231, University of Burgundy Franche-Comté, 15 Boulevard Maréchal de Lattre de Tassigny, 21070 Dijon, France.

Int J Mol Sci ; 23(19)2022 Sep 29.

Article de En | MEDLINE | ID: mdl-36232804

Sujet(s)
Mots clés

CHARGE syndrome; CHD7; dysgenesis of the corpus callosum; mouse models; neurodevelopmental disorders

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Protéines de liaison à l'ADN / Syndrome CHARGE Type d'étude: Diagnostic_studies / Prognostic_studies Limites: Animals Langue: En Journal: Int J Mol Sci Année: 2022 Type de document: Article Pays d'affiliation: France

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