» Articles » PMID: 1345170

Linkage Disequilibrium Mapping in Isolated Founder Populations: Diastrophic Dysplasia in Finland

Overview
Journal Nat Genet
Specialty Genetics
Date 1992 Nov 1
PMID 1345170
Citations 185
Authors
Affiliations
Soon will be listed here.
Abstract

Linkage disequilibrium mapping in isolated populations provides a powerful tool for fine structure localization of disease genes. Here, Luria and Delbrück's classical methods for analysing bacterial cultures are adapted to the study of human isolated founder populations in order to estimate (i) the recombination fraction between a disease locus and a marker; (ii) the expected degree of allelic homogeneity in a population; and (iii) the mutation rate of marker loci. Using these methods, we report striking linkage disequilibrium for diastrophic dysplasia (DTD) in Finland indicating that the DTD gene should lie within 0.06 centimorgans (or about 60 kilobases) of the CSF1R gene. Predictions about allelic homogeneity in Finland and mutation rates in simple sequence repeats are confirmed by independent observations.

Citing Articles

X-linked hydrocephalus genes: Their proximity to telomeres and high A + T content compared to Parkinson's disease.

Hart M, Conrad J, Barrett E, Legg K, Ivey G, Lee P Exp Neurol. 2023; 366:114433.

PMID: 37156332 PMC: 10330542. DOI: 10.1016/j.expneurol.2023.114433.


Mutability of druggable kinases and pro-inflammatory cytokines by their proximity to telomeres and A+T content.

McKnight I, Raines R, White H, Nosoudi N, Lee C, Lee P PLoS One. 2023; 18(4):e0283470.

PMID: 37104389 PMC: 10138820. DOI: 10.1371/journal.pone.0283470.


Translating non-coding genetic associations into a better understanding of immune-mediated disease.

Stankey C, Lee J Dis Model Mech. 2023; 16(3.

PMID: 36897113 PMC: 10040244. DOI: 10.1242/dmm.049790.


Familial amyloidosis of the Finnish type: clinical and neurophysiological features of two index cases.

Antunes Cunha I, Bras A, Silva F, Matos A BMJ Case Rep. 2022; 15(11).

PMID: 36379630 PMC: 9668035. DOI: 10.1136/bcr-2021-245764.


Drug-Targeted Genomes: Mutability of Ion Channels and GPCRs.

Raines R, McKnight I, White H, Legg K, Lee C, Li W Biomedicines. 2022; 10(3).

PMID: 35327396 PMC: 8945769. DOI: 10.3390/biomedicines10030594.