BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells.

Lessel, Davor; Gehbauer, Christina; Bramswig, Nuria C; Schluth-Bolard, Caroline; Venkataramanappa, Sathish; van Gassen, Koen L I; Hempel, Maja; Haack, Tobias B; Baresic, Anja; Genetti, Casie A; Funari, Mariana F A; Lessel, Ivana; Kuhlmann, Leonie; Simon, Ruth; Liu, Pentao; Denecke, Jonas; Kuechler, Alma; de Kruijff, Ineke; Shoukier, Moneef; Lek, Monkol; Mullen, Thomas; Lüdecke, Hermann-Josef; Lerario, Antonio M; Kobbe, Robin; Krieger, Thorsten; Demeer, Benedicte; Lebrun, Marine; Keren, Boris; Nava, Caroline; Buratti, Julien; Afenjar, Alexandra; Shinawi, Marwan; Guillen Sacoto, Maria J; Gauthier, Julie; Hamdan, Fadi F; Laberge, Anne-Marie; Campeau, Philippe M; Louie, Raymond J; Cathey, Sara S; Prinz, Immo; Jorge, Alexander A L; Terhal, Paulien A; Lenhard, Boris; Wieczorek, Dagmar; Strom, Tim M; Agrawal, Pankaj B; Britsch, Stefan; Tolosa, Eva; Kubisch, Christian.
Brain; 2018 Jul 09.
Artigo em Inglês | MEDLINE | ID: mdl-29985992

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