BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells
Davor Lessel(Universität Hamburg), Christian Kubisch(University of Bonn), Mariana F.A. Funari(Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo), Paulien A. Terhal(University Medical Center Utrecht), Boris Keren(Sorbonne Université), Thorsten Krieger(Universität Hamburg), Marine Lebrun(Hôpital Nord), Tobias B. Haack(Technical University of Munich), Eva Tolosa(Universität Hamburg), Pentao Liu(Wellcome/MRC Cambridge Stem Cell Institute), Nuria C. Bramswig(Düsseldorf University Hospital), Julien Buratti(Sorbonne Université), Monkol Lek(Massachusetts General Hospital), Immo Prinz(Universität Hamburg), Sathish Venkataramanappa(Universität Ulm), Ivana Lessel(Universität Hamburg), Jonas Denecke(Universität Hamburg), Ineke de Kruijff(St. Antonius Ziekenhuis), Sara Cathey(Greenwood Genetic Center), Caroline Nava(Centre National de la Recherche Scientifique), Caroline Schluth‐Bolard(Université Claude Bernard Lyon 1), Moneef Shoukier(München Klinik), Koen L.I. van Gassen(University Medical Center Utrecht), Raymond J. Louie(Greenwood Genetic Center), Boris Lenhard(Imperial Valley College), Alexander A.L. Jorge(Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo), Bénédicte Demeer(Centre Hospitalier Universitaire Amiens-Picardie), Leonie Kuhlmann(Medizinische Hochschule Hannover), Antônio Marcondes Lerário(University of Michigan), Maja Hempel(Helmholtz Zentrum München), Robin Kobbe(Universität Hamburg), Dagmar Wieczorek(Essen University Hospital), María J. Guillen Sacoto, Anne‐Marie Laberge(Centre Hospitalier Universitaire Sainte-Justine), Pankaj B. Agrawal(Post Graduate Institute of Medical Education and Research), Christina Gehbauer(Universität Hamburg), Stefan Britsch(Universität Ulm), Casie A. Genetti(Boston Children's Hospital), Philippe M. Campeau(Centre Hospitalier Universitaire Sainte-Justine), Fadi F. Hamdan(Centre Hospitalier Universitaire Sainte-Justine), Thomas E. Mullen(Broad Institute), Julie Gauthier(Centre Hospitalier Universitaire Sainte-Justine), Alexandra Afenjar(Sorbonne Université), Tim M. Strom(Ludwig-Maximilians-Universität München), Hermann‐Josef Lüdecke(Düsseldorf University Hospital), Ruth Simon(City of Hope), Anja Barešić(MRC London Institute of Medical Sciences), Alma Kuechler(Essen University Hospital), Marwan Shinawi(St. Louis Children's Hospital)
Cited by 133
Related Papers
Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics
|Nature Communications|2018|1.2k
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
|Nature Genetics|2006|1.2k
A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets
|Nature Genetics|1995|1.1k
A Potassium Channel Mutation in Neonatal Human Epilepsy
|Science|1998|1.1k