Replicable in vivo physiological and behavioral phenotypes of the Shank3B null mutant mouse model of autism-Reference-Cited by-同舟云学术

Replicable in vivo physiological and behavioral phenotypes of the Shank3B null mutant mouse model of autism

Published:2017-06-15 Issue:1 Volume:8 Page:
ISSN:2040-2392
Container-title:Molecular Autism
language:en
Short-container-title:Molecular Autism

Author:

Dhamne Sameer C.,Silverman Jill L.,Super Chloe E.,Lammers Stephen H. T.,Hameed Mustafa Q.,Modi Meera E.,Copping Nycole A.,Pride Michael C.,Smith Daniel G.,Rotenberg Alexander,Crawley Jacqueline N.,Sahin Mustafa^ORCID

Funder

Autism Speaks

National Institutes of Health

Publisher

Springer Science and Business Media LLC

Subject

Psychiatry and Mental health,Developmental Biology,Developmental Neuroscience,Molecular Biology

Link

http://link.springer.com/content/pdf/10.1186/s13229-017-0142-z.pdf

Reference77 articles.

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2. Gauthier J, et al. Novel de novo SHANK3 mutation in autistic patients. Am J Med Genet B Neuropsychiatr Genet. 2009;150B(3):421–4.

3. Qin J, et al. Association study of SHANK3 gene polymorphisms with autism in Chinese Han population. BMC Med Genet. 2009;10:61.

4. Kolevzon A, et al. Analysis of a purported SHANK3 mutation in a boy with autism: clinical impact of rare variant research in neurodevelopmental disabilities. Brain Res. 2011;1380:98–105.

5. Durand CM, et al. Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders. Nat Genet. 2007;39(1):25–7.

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