The tRNA(Gln) 4336 mitochondrial DNA variant is not a high penetrance mutation which predisposes to dementia before the age of 75 years. (Q33678113)

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31 October 2019

title

The tRNA(Gln) 4336 mitochondrial DNA variant is not a high penetrance mutation which predisposes to dementia before the age of 75 years (English)

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31 October 2019

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1 reference

3

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31 October 2019

Tom Dening

4

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31 October 2019

author name string

C Tysoe

1

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31 October 2019

D Robinson

2

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31 October 2019

E S Paykel

5

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31 October 2019

F A Huppert

6

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31 October 2019

D C Rubinsztein

7

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31 October 2019

language of work or name

English

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publication date

1 December 1996

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Journal of Medical Genetics

31 October 2019

published in

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31 October 2019

volume

33

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31 October 2019

issue

12

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31 October 2019

page(s)

1002-1006

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Mutagenically separated PCR (MS-PCR): a highly specific one step procedure for easy mutation detection

31 October 2019

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Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

21 June 2018

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21 June 2018

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A mitochondrial DNA clone is associated with increased risk for Alzheimer disease

21 June 2018

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Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

21 June 2018

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Sequence and organization of the human mitochondrial genome

21 June 2018

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The association between quantitative measures of dementia and of senile change in the cerebral grey matter of elderly subjects.

21 June 2018

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CAMDEX. A standardised instrument for the diagnosis of mental disorder in the elderly with special reference to the early detection of dementia.

21 June 2018

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21 June 2018

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A computerized psychiatric diagnostic system and case nomenclature for elderly subjects: GMS and AGECAT.

21 June 2018

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Alterations in calcium content and biochemical processes in cultured skin fibroblasts from aged and Alzheimer donors

21 June 2018

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Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein gene

21 June 2018

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A mutation in the amyloid precursor protein associated with hereditary Alzheimer's disease

21 June 2018

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Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

21 June 2018

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The MRC Multicentre Study of Cognitive Function and Ageing: a EURODEM incidence study in progress

21 June 2018

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Diseases of the mitochondrial DNA.

21 June 2018

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Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14

21 June 2018

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Mapping of a gene predisposing to early-onset Alzheimer's disease to chromosome 14q24.3

21 June 2018

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Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14.

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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30 October 2018

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Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder.

30 October 2018

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Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with HhaI

30 October 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/9004131

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Cytochrome oxidase deficiency in Alzheimer's disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9004131

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.33.12.1002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9004131%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

1 reference

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31 October 2019

PubMed publication ID

9004131

1 reference