LINKAGE DISEQUILIBRIUM DETECTED BETWEEN MYOTONIC-DYSTROPHY AND THE ANONYMOUS MARKER D19S63 IN THE SPANISH POPULATION

被引:0
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作者
COBO, A
GRINBERG, D
BALCELLS, S
VILAGELIU, L
GONZALEZDUARTE, R
BAIGET, M
机构
[1] HOSP SANTA CRUZ & SAN PABLO,MOLEC GENET UNIT,AVE ST ANTONI MA CLARET 167,E-08025 BARCELONA,SPAIN
[2] UNIV BARCELONA,FAC BIOL,DEPT GENET,E-08071 BARCELONA,SPAIN
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暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We used the following polymorphic markers: APOC2 (BanI, BglI, TaqI), CKMM (NcoI, TaqI), and D19S63 (PstI) to haplotype 33 Spanish myotonic dystrophy (DM) families. We analysed the allele and haplotype frequencies of our sample, and the possible association of alleles or haplotypes with the disease. We found a slight linkage disequilibrium between APOC2 (BanI) and DM, but no disequilibrium when using all other APOC2 and CKMM RFLPs; this agrees with data previously reported. In addition, we found a very strong linkage disequilibrium when using D19S63 (PstI), the + allele being associated with the DM locus. This disequilibrium in the Spanish population indicates that D19S63 is very close to the DM locus.
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页码:287 / 291
页数:5
相关论文
共 24 条
  • [1] THE ANONYMOUS MARKER D19S63 SHOWS LINKAGE DISEQUILIBRIUM WITH MYOTROPIC DYSTROPHY (DM) IN THE SPANISH POPULATION
    COBO, AM
    BALCELLS, S
    GRINBERG, D
    GONZALEZDUARTE, R
    BAIGET, M
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (04) : 335 - 335
  • [2] DETECTION OF LINKAGE DISEQUILIBRIUM BETWEEN THE MYOTONIC-DYSTROPHY LOCUS AND A NEW POLYMORPHIC DNA MARKER
    HARLEY, HG
    BROOK, JD
    FLOYD, J
    RUNDLE, SA
    CROW, S
    WALSH, KV
    THIBAULT, MC
    HARPER, PS
    SHAW, DJ
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (01) : 68 - 75
  • [3] ANALYSIS OF MYOTONIC-DYSTROPHY FAMILIES REVEALS NO LINKAGE DISEQUILIBRIUM IN THE FRENCH POPULATION BETWEEN DM AND CLOSELY LINKED MARKERS
    LAVEDAN, C
    BOILEAU, C
    BONAITIPELLIE, C
    DUROS, C
    SIMON, M
    SAVOY, D
    JOHNSON, K
    JUNIEN, C
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (04) : 499 - 499
  • [4] A CHROMOSOME-19 CLONE FROM A TRANSLOCATION BREAKPOINT SHOWS CLOSE LINKAGE AND LINKAGE DISEQUILIBRIUM WITH MYOTONIC-DYSTROPHY
    KORNELUK, RG
    MACLEOD, HL
    MCKEITHAN, TW
    BROOKS, JD
    MACKENZIE, AE
    [J]. GENOMICS, 1989, 4 (02) : 146 - 151
  • [5] GENETIC-LINKAGE BETWEEN THE LOCI FOR MYOTONIC-DYSTROPHY AND PEPTIDASE-D
    OBRIEN, T
    BALL, S
    SARFARAZI, M
    HARPER, PS
    ROBSON, EB
    [J]. ANNALS OF HUMAN GENETICS, 1983, 47 (MAY) : 117 - 121
  • [6] DETECTION OF LINKAGE DISEQUILIBRIUM BETWEEN THE MYOTONIC-DYSTROPHY LOCUS AND 4 DNA POLYMORPHISMS IN EUROPEAN AND OTHER POPULATIONS
    HARLEY, HG
    BROOK, JD
    RUNDLE, SA
    CROW, S
    THIBAULT, MC
    MIKI, T
    ABELIOVICH, D
    SANDKUIJL, LA
    SNELL, RG
    HARPER, PS
    SHAW, DJ
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (04) : 342 - 342
  • [7] LINKAGE ANALYSIS OF THE APOLIPOPROTEIN-C2 GENE AND MYOTONIC-DYSTROPHY ON HUMAN CHROMOSOME-19 REVEALS LINKAGE DISEQUILIBRIUM IN A FRENCH-CANADIAN POPULATION
    MACKENZIE, AE
    MACLEOD, HL
    HUNTER, AGW
    KORNELUK, RG
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1989, 44 (01) : 140 - 147
  • [8] PHYSICAL AND GENETIC-MAPPING OF A NOVEL CHROMOSOME-19 ERCC1 MARKER SHOWING CLOSE LINKAGE WITH MYOTONIC-DYSTROPHY
    SHUTLER, G
    MACKENZIE, AE
    BRUNNER, H
    WIERINGA, B
    DEJONG, P
    LOHMAN, FP
    LEBLOND, S
    BAILLY, J
    KORNELUK, RG
    [J]. GENOMICS, 1991, 9 (03) : 500 - 504
  • [9] CLOSE LINKAGE OF THE JAPANESE MYOTONIC MUSCULAR-DYSTROPHY LOCUS TO D19S19
    MIKI, T
    TAKEMOTO, Y
    NISHIKAWA, K
    NAKURA, J
    KAMINO, K
    TAKAI, S
    OGIHARA, T
    [J]. CYTOGENETICS AND CELL GENETICS, 1989, 51 (1-4): : 1044 - 1044
  • [10] D19S51 IS CLOSELY LINKED WITH AND MAPS DISTAL TO THE MYOTONIC-DYSTROPHY LOCUS ON 19Q
    TSILFIDIS, C
    MACKENZIE, AE
    SHUTLER, G
    LEBLOND, S
    BAILLY, J
    JOHNSON, K
    WILLIAMSON, R
    SIEGELBARTELT, J
    KORNELUK, RG
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (05) : 961 - 965