Work

Cognitive deficits in the Snord116 deletion mouse model for Prader-Willi syndrome

Year: 2018

Type: review

Source: Neurobiology of Learning and Memory

DOI: 10.1016/j.nlm.2018.05.011

Authors: Anna Adhikari, Nycole A. Copping, Beth Onaga, Michael C. Pride, Rochelle L. Coulson, Mu Yang, Dag H. Yasui, Janine M. LaSalle, Jill L. Silverman

Institutions: University of California Davis Medical Center, University of California, Davis

Language: English

Topic: Genetic Syndromes and Imprinting

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: National Institutes of Health, National Institute of Neurological Disorders and Stroke, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G1105165173, MIND Institute Intellectual and Developmental Disabilities Research Center, G5417353852, Imprinted snoRNA loci and circadian entrainment, MIND Institute Intellectual and Developmental Disabilities Research Center, Phenotypic Characterization of Novel Models of Dup15q Syndrome

OpenAlex ID: W2803711209

FWCI: 1.651

Cites: 59

Cited by: 76

Related to: 10