Heterozygous deletion of the Williams-Beuren syndrome critical interval in mice recapitulates most features of the human disorder

Human molecular genetics

Volumn 23, Issue 24, 2014, Pages 6481-6494

  Segura Puimedon, Maria ^a   Sahún, Ignasi ^a   Velot, Emilie ^a   Dubus, Pierre ^a   Borralleras, Cristina ^a   Rodrigues, Ana J ^a   Valero, María C ^a   Valverde, Olga ^a   Sousa, Nuno ^a   Herault, Yann ^a   Dierssen, Mara ^a   Pérez Jurado, Luis A ^a   Campuzano, Victoria ^a  

^a UNIVERSITAT POMPEU FABRA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; ANIMAL BEHAVIOR; BODY WEIGHT; BRAIN; CARDIOMEGALY; CHROMOSOME; CHROMOSOME 7; CHROMOSOME DELETION; CRANIOFACIAL MALFORMATION; DISEASE MODEL; FEMALE; GENE DOSAGE; GENETICS; HETEROZYGOTE; HUMAN; HYPERTENSION; KNOCKOUT MOUSE; LETHAL GENE; MALE; MOUSE; NERVE CELL; ORGAN SIZE; PATHOLOGY; PATHOPHYSIOLOGY; SYNTENY; WILLIAMS BEUREN SYNDROME;

ANIMALS; BEHAVIOR, ANIMAL; BODY WEIGHT; BRAIN; CARDIOMEGALY; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 7; CHROMOSOMES, MAMMALIAN; CRANIOFACIAL ABNORMALITIES; DISEASE MODELS, ANIMAL; FEMALE; GENE DOSAGE; GENES, LETHAL; HETEROZYGOTE; HUMANS; HYPERTENSION; MALE; MICE; MICE, KNOCKOUT; NEURONS; ORGAN SIZE; SYNTENY; WILLIAMS SYNDROME;

EID: 84930629892     PISSN: None     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddu368     Document Type: Article

References (0)