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Volumn 50, Issue 3, 2018, Pages 329-332
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Correction: BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange-like syndrome (Nature Genetics DOI: 10.1038/s41588-018-0042-y);BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange-like syndrome
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Author keywords
[No Author keywords available]
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Indexed keywords
PROTEIN;
PROTEIN BRD4;
PROTEIN NIPBL;
UNCLASSIFIED DRUG;
BRD4 PROTEIN, HUMAN;
NIPBL PROTEIN, HUMAN;
NUCLEAR PROTEIN;
PROTEIN BINDING;
TRANSCRIPTION FACTOR;
ANIMAL CELL;
ARTICLE;
CLINICAL ARTICLE;
CONTROLLED STUDY;
DE LANGE SYNDROME;
EMBRYO;
ENHANCER REGION;
GENE EXPRESSION;
GENE MUTATION;
GENETIC VARIABILITY;
HAPLOINSUFFICIENCY;
HETEROZYGOTE;
HISTONE ACETYLATION;
HUMAN;
MOUSE;
NONHUMAN;
PHENOTYPE;
PRIORITY JOURNAL;
PROTEIN BINDING;
PROTEIN PROTEIN INTERACTION;
ANIMAL;
BINDING SITE;
CASE REPORT;
CELL CULTURE;
CHILD;
FEMALE;
GENE EXPRESSION REGULATION;
GENETICS;
MALE;
METABOLISM;
MISSENSE MUTATION;
PEDIGREE;
PRESCHOOL CHILD;
TRANSGENIC MOUSE;
ANIMALS;
BINDING SITES;
CELLS, CULTURED;
CHILD;
CHILD, PRESCHOOL;
DE LANGE SYNDROME;
ENHANCER ELEMENTS, GENETIC;
FEMALE;
GENE EXPRESSION REGULATION, DEVELOPMENTAL;
HAPLOINSUFFICIENCY;
HUMANS;
MALE;
MICE;
MICE, TRANSGENIC;
MUTATION, MISSENSE;
NUCLEAR PROTEINS;
PEDIGREE;
PHENOTYPE;
PROTEIN BINDING;
PROTEINS;
TRANSCRIPTION FACTORS;
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EID: 85041131192
PISSN: 10614036
EISSN: 15461718
Source Type: Journal
DOI: 10.1038/s41588-018-0069-0 Document Type: Erratum |
Times cited : (97)
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References (37)
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