Combination of Linkage Mapping and Microarray-Expression Analysis Identifies NF-κB Signaling Defect as a Cause of Autosomal-Recessive Mental Retardation

American Journal of Human Genetics

Volumn 85, Issue 6, 2009, Pages 903-908

  Philippe, Orianne ^a   Rio, Marlène ^a   Carioux, Astrid ^b   Plaza, Jean Marc ^c   Guigue, Philippe ^a   Molinari, Florence ^a   Boddaert, Nathalie ^a   Bole Feysot, Christine ^b   Nitschke, Patrick ^c   Smahi, Asma ^a   Munnich, Arnold ^a   Colleaux, Laurence ^a  

^a INSERM   (France)

^b IMAGINE INSTITUTE   (France)

^c UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

I KAPPA B ALPHA; I KAPPA B KINASE; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; RNA; TUMOR NECROSIS FACTOR ALPHA;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CHILD; CONTROLLED STUDY; GENE; GENE EXPRESSION; GENE EXPRESSION PROFILING; GENE IDENTIFICATION; GENE MAPPING; GENE SEQUENCE; GENETIC LINKAGE; HUMAN; HUMAN CELL; HUMAN CELL CULTURE; MALE; MENTAL DEFICIENCY; MICROCEPHALY; NONSENSE MUTATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; PROTEIN DEGRADATION; SIGNAL TRANSDUCTION; SKIN FIBROBLAST; TRAPPC9 GENE; WHITE MATTER;

EID: 71449106786     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ajhg.2009.11.007     Document Type: Article

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