No mitochondrial haplotype was found to increase risk for Alzheimer's disease.

doi:10.1016/s0006-3223(97)00461-7

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Back to search

Article

No mitochondrial haplotype was found to increase risk for Alzheimer's disease.

Biological psychiatry - 1 Sept 1998

Zsurka G, Kálmán J, Császár A, Raskó I, Janka Z, Venetianer P

Abstract excerpt

BACKGROUND: Seventy Alzheimer's disease (AD) patients and 80 age- and sex-matched controls were analyzed for mitochondrial mutations T4336C and A3397G, reported to be associated with AD, and for mutations T4216C/G13708A characteristic for a normal human haplotype associated with increased frequency of occurrence of some hereditary diseases. The distribution of apolipoprotein E (apoE) alleles was also analyzed....

Topics

Aged
Alleles
Alzheimer Disease
Female
Genotype
Haplotypes
Humans
Male
Mitochondria
Mutation
Risk Factors

Source

Open in PubMed

Identifiers

PMID: 9755361
DOI: 10.1016/s0006-3223(97)00461-7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics