Identification of genetic variants of LGI1 and RTN4R (NgR1) linked to schizophrenia that are defective in NgR1-LGI1 signaling.

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第一作者： Rhalena A,Thomas

第一单位： Department of Neurology and Neurosurgery Montreal Neurological Institute McGill University 3801 University Montreal Quebec H3A 2B4 Canada.

作者： Rhalena A,Thomas ^[1] ; Amirthagowri,Ambalavanan ^[2] ; Guy A,Rouleau ^[3] ; Philip A,Barker ^[4]

作者单位： Department of Neurology and Neurosurgery Montreal Neurological Institute McGill University 3801 University Montreal Quebec H3A 2B4 Canada. ^[1] Department of Human Genetics McGill University 1205 Dr Penfield Avenue Montreal Quebec H3A 1B1 Canada. ^[2] Department of Neurology and NeurosurgeryMontreal Neurological InstituteMcGill University3801 UniversityMontrealQuebecH3A 2B4Canada; Department of Human GeneticsMcGill University1205 Dr Penfield AvenueMontrealQuebecH3A 1B1Canada. ^[3] Department of Neurology and NeurosurgeryMontreal Neurological InstituteMcGill University3801 UniversityMontrealQuebecH3A 2B4Canada; Department of BiologyUniversity of British ColumbiaKelownaBC. V1V 1V7Canada. ^[4]

关键词 LGI1 NgR1 RTN4R RhoA schizophrenia synapse formation

DOI 10.1002/mgg3.215

PMID 27468420

发布时间 2018-11-13

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Molecular genetics & genomic medicine

2016年4卷4期

447-56页

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Identification of genetic variants of LGI1 and RTN4R (NgR1) linked to schizophrenia that are defective in NgR1-LGI1 signaling.

Molecular genetics & genomic medicine

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Molecular genetics & genomic medicine

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Identification of genetic variants of LGI1 and RTN4R (NgR1) linked to schizophrenia that are defective in NgR1-LGI1 signaling.

Molecular genetics & genomic medicine

相似文献

Molecular genetics & genomic medicine

相关期刊

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