Amyloid precursor protein mutation at codon 713 (Ala → Val) does not cause schizophrenia: non-pathogenic variant found at codon 705 (silent)
- 23 January 1995
- journal article
- Published by Elsevier in Neuroscience Letters
- Vol. 184 (2) , 90-93
- https://doi.org/10.1016/0304-3940(94)11176-j
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- C to T nucleotide substitution in codon 713 of amyloid precursor protein gene not found in 86 unrelated schizophrenics from multiplex familiesAmerican Journal of Medical Genetics, 1993
- A novel silent variant at codon 711 and a variant at codon 708 of the APP sequence detected in Spanish Alzheimer and control casesNeuroscience Letters, 1993
- More missense in amyloid geneNature Genetics, 1992
- A novel mutation in the ?-protein coding region of the amyloid ?-protein precursor (APP) geneHuman Genetics, 1992
- Screening for mutations in the open reading frame and promoter of the β-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val→lleHuman Molecular Genetics, 1992
- Prevalence of Alzheimer's disease and other dementias in an elderly urban populationNeurology, 1991
- Early-onset Alzheimer's disease caused by mutations at codon 717 of the β-amyloid precursor protein geneNature, 1991
- Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's diseaseNature, 1991
- Alzheimer's disease: Initial report of the purification and characterization of a novel cerebrovascular amyloid proteinBiochemical and Biophysical Research Communications, 1984
- “Mini-mental state”Journal of Psychiatric Research, 1975