TY - JOUR
T1 - Evidence of linkage disequilibrium in the Spanish polycystic kidney disease I population
AU - Peral, Belén
AU - Ward, Christopher J.
AU - San Millán, José L.
AU - Thomas, Sandra
AU - Stallings, Raymond L.
AU - Moreno, Felipe
AU - Harris, Peter C.
PY - 1994/5/17
Y1 - 1994/5/17
N2 - Forty-one Spanish families with polycystic kidney disease 1 (PKD1) were studied for evidence of linkage disequilibrium between the disease locus and six closely linked markers. Four of these loci-three highly polymorphic microsatellites (SM6, CW3, and CW2) and an RFLP marker (Blu24)-are described for the first time in this report. Overall the results reveal many different haplotypes on the disease-carrying chromosome, suggesting a variety of independent PKD1 mutations. However, linkage disequilibrium was found between BLu24 and PKD1, and this was corroborated by haplotype analysis including the microsatellite polymorphisms. From this analysis a group of closely related haplotypes, consisting of four markers, was found on 40% of PKD1 chromosomes, although markers flanking this homogeneous region showed greater variability. This study has highlighted an interesting subpopulation of Spanish PKD1 chromosomes, many of which have a common origin, that may be useful for localizing the PKD1 locus more precisely.
AB - Forty-one Spanish families with polycystic kidney disease 1 (PKD1) were studied for evidence of linkage disequilibrium between the disease locus and six closely linked markers. Four of these loci-three highly polymorphic microsatellites (SM6, CW3, and CW2) and an RFLP marker (Blu24)-are described for the first time in this report. Overall the results reveal many different haplotypes on the disease-carrying chromosome, suggesting a variety of independent PKD1 mutations. However, linkage disequilibrium was found between BLu24 and PKD1, and this was corroborated by haplotype analysis including the microsatellite polymorphisms. From this analysis a group of closely related haplotypes, consisting of four markers, was found on 40% of PKD1 chromosomes, although markers flanking this homogeneous region showed greater variability. This study has highlighted an interesting subpopulation of Spanish PKD1 chromosomes, many of which have a common origin, that may be useful for localizing the PKD1 locus more precisely.
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M3 - Article
C2 - 7909986
AN - SCOPUS:0028297233
SN - 0002-9297
VL - 54
SP - 899
EP - 908
JO - American journal of human genetics
JF - American journal of human genetics
IS - 5
ER -