Identification of genetic variants of LGI 1 and RTN 4R (NgR1) linked to schizophrenia that are defective in NgR1– LGI 1 signaling-Reference-Cited by-同舟云学术

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Identification of genetic variants of LGI 1 and RTN 4R (NgR1) linked to schizophrenia that are defective in NgR1– LGI 1 signaling

Published:2016-03-11 Issue:4 Volume:4 Page:447-456
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Thomas Rhalena A.¹,Ambalavanan Amirthagowri²,Rouleau Guy A.¹²,Barker Philip A.¹³

Affiliation:

1. Department of Neurology and Neurosurgery Montreal Neurological Institute McGill University 3801 University Montreal Quebec H3A 2B4 Canada

2. Department of Human Genetics McGill University 1205 Dr Penfield Avenue Montreal Quebec H3A 1B1 Canada

3. Department of Biology University of British Columbia Kelowna BC. V1V 1V7 Canada

Funder

Canadian Institutes of Health Research

Fonds de Recherche du Québec - Santé

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.215

Reference55 articles.

1. Anatomical Plasticity of Adult Brain Is Titrated by Nogo Receptor 1

2. De novo variants in sporadic cases of childhood onset schizophrenia;Ambalavanan A.;Eur. J. Hum. Genet.,2015

3. Direct Measure of the De Novo Mutation Rate in Autism and Schizophrenia Cohorts

4. Genetics of Schizophrenia and the New Millennium: Progress and Pitfalls

5. A novel three base-pair LGI1 deletion leading to loss of function in a family with autosomal dominant lateral temporal epilepsy and migraine-like episodes

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