Deficits in early neural tube identity found in CHARGE syndrome

eLife

Volumn 2013, Issue 2, 2013, Pages

  Haldipur, Parthiv ^a   Millen, Kathleen J ^a,b  

^a SEATTLE CHILDREN S RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHD7 PROTEIN; FIBROBLAST GROWTH FACTOR 8; GASTRULATION BRAIN HOMEOBOX 2; NUCLEIC ACID BINDING PROTEIN; TRANSCRIPTION FACTOR OTX2; UNCLASSIFIED DRUG; FGF8 PROTEIN, MOUSE; GBX2 PROTEIN, MOUSE; HOMEODOMAIN PROTEIN; OTX2 PROTEIN, MOUSE; TRANSCRIPTION FACTOR OTX;

ARTICLE; BRAIN STEM RESPONSE; CENTRAL NERVOUS SYSTEM FUNCTION; CHILD; CHROMATIN IMMUNOPRECIPITATION; GENE EXPRESSION; GENE MUTATION; GENETIC ANALYSIS; HUMAN; NEURAL TUBE DEFECT; NEUROIMAGING; NEUROPHYSIOLOGY; SIGNAL TRANSDUCTION; SYNDROME CHARGE; ANIMAL; CEREBELLUM VERMIS; METABOLISM;

ANIMALS; CEREBELLAR VERMIS; CHARGE SYNDROME; FIBROBLAST GROWTH FACTOR 8; HOMEODOMAIN PROTEINS; HUMANS; OTX TRANSCRIPTION FACTORS;

EID: 84891535954     PISSN: None     EISSN: 2050084X     Source Type: Journal    
DOI: 10.7554/eLife.01873     Document Type: Article

References (11)

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