Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutation

Author:

Carroll Liam S.,Woolf Rebecca,Ibrahim Yousef,Williams Hywel J.,Dwyer Sarah,Walters James,Kirov George,O’Donovan Michael C.,Owen Michael J.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Biological Psychiatry,Psychiatry and Mental health,Genetics(clinical),Genetics

Reference12 articles.

1. Predicting functional effect of human missense mutations using PolyPhen-2.;Adzhubei;Curr Protoc Hum Genet,2013

2. Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia.;Carroll;Am J Med Genet B Neuropsychiatr Genet,2011

3. Microdeletion syndromes.;Carvill;Curr Opin Genet Dev,2013

4. Mutation screening of the DTNBP1 exonic sequence in 669 schizophrenics and 710 controls using high-resolution melting analysis.;Dwyer;Am J Med Genet B Neuropsychiatr Genet,2010

5. Dynamic compartmentalization of the voltage-gated sodium channels in axons.;Garrido;Biol Cell,2003

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