C to T nucleotide substitution in codon 713 of amyloid precursor protein gene not found in 86 unrelated schizophrenics from multiplex families-Reference-Cited by-同舟云学术

C to T nucleotide substitution in codon 713 of amyloid precursor protein gene not found in 86 unrelated schizophrenics from multiplex families

Published:1993-05-01 Issue:1 Volume:48 Page:36-39
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Coon Hilary,Hoff Mark,Holik John,Delisi Lynn E.,Crowe Timothy,Freedman Robert,Shields Gail,Boccio Angela M.,Lerman Melissa,Gershon Elliot S.,Gejman Pablo V.,Leppert Mark,Byerley William

Publisher

Wiley

Subject

Genetics(clinical)

Reference27 articles.

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2. Polymorphic DNA region adjacent to the 5' end of the human insulin gene.

3. (1972): “The Schizophrenic Disorders: Long-Term Patient and Family Studies.” New Haven: Yale University Press.

4. Three Lectures on Schizophrenia

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1. Protein expression of targets of the FMRP regulon is altered in brains of subjects with schizophrenia and mood disorders;Schizophrenia Research;2015-07

2. A family with Alzheimer disease and strokes associated with A713T mutation of the APP gene;Neurology;2004-09-13

3. An interstitial deletion of the long arm of chromosome 21 in a case of a first episode of psychosis;Acta Psychiatrica Scandinavica;2002-07

4. Amyloid precursor protein mutation at codon 713 (Ala → Val) does not cause schizophrenia: non-pathogenic variant found at codon 705 (silent);Neuroscience Letters;1995-01

5. Schizophrenia and APP gene mutations;Biological Psychiatry;1995-01