Assignment of the tibial muscular dystrophy (TMD) locus on chromosome 2q31.

被引:0
|
作者
Haravuori, H
Mäkelä-Bengs, P
Udd, B
Pulkkinen, L
Partanen, J
Somer, H
Peltonen, L
机构
[1] Natl Publ Hlth Inst, Dept Human Mol Genet, Helsinki, Finland
[2] Vaasa Cent Hosp, Dept Neurol, Vaasa, Finland
[3] Univ Kuopio, Cent Hosp, Dept Clin Neurophysiol, Kuopio, Finland
[4] Univ Helsinki, Cent Hosp, Dept Neurol, Helsinki, Finland
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
144
引用
收藏
页码:A29 / A29
页数:1
相关论文
共 50 条
  • [1] Assignment of the tibial muscular dystrophy locus to chromosome 2q31
    Haravuori, H
    Makela-Bengs, P
    Udd, B
    Partanen, J
    Pulkkinen, L
    Somer, H
    Peltonen, L
    AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (03) : 620 - 626
  • [2] Tibial muscular dystrophy - haplotype analysis of 150 Finnish patients and physical region of chromosome 2q31.
    Haravuori, H
    Udd, B
    Somer, H
    Peltonen, L
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 333 - 333
  • [3] Tibial muscular dystrophy - from clinical description to linkage on chromosome 2q31
    Udd, B
    Haravuori, H
    Kalimo, H
    Partanen, J
    Pulkkinen, L
    Paetau, A
    Peltonen, L
    Somer, H
    NEUROMUSCULAR DISORDERS, 1998, 8 (05) : 327 - 332
  • [4] Tibial muscular dystrophy (TMD), 2q31 linked myopathy:: Sequencing and functional studies of the titin (TTN) gene
    Hackman, P
    Richard, I
    Vihola, A
    Haravuori, H
    Marchand, S
    Labeit, S
    Sarparanta, J
    Taivainen, A
    Carpén, O
    Udd, B
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2002, 199 : S35 - S35
  • [5] Tibial muscular dystrophy and late-onset distal myopathy are linked to the same locus on chromosome 2q
    Haravuori, H
    Mäkelä-Bengs, P
    Figlewicz, DA
    Udd, B
    Somer, H
    Griggs, RC
    Peltonen, L
    NEUROLOGY, 1998, 50 (04) : A186 - A186
  • [6] Tibial muscular dystrophy - analysis of the chromosome 2q linked physical region
    Haravuori, H
    Udd, B
    Hackman, P
    Somer, H
    Peltonen, L
    NEUROMUSCULAR DISORDERS, 2001, 11 (6-7) : 653 - 653
  • [7] A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: Evidence for another limb-girdle muscular dystrophy locus
    Weiler, T
    Greenberg, CR
    Zelinski, T
    Nylen, E
    Coghlan, G
    Crumley, MJ
    Fujiwara, TM
    Morgan, K
    Wrogemann, K
    AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (01) : 140 - 147
  • [8] Tibial muscular dystrophy (TMD/LGMD2J) - titin gene defects and functional genomics
    Hackman, P
    Vihola, A
    Sarparanta, J
    Haravuori, H
    Marchand, S
    de Seze, J
    Van den Bergh, P
    Labeit, S
    Witt, C
    Richard, I
    Udd, B
    NEUROMUSCULAR DISORDERS, 2003, 13 (7-8) : 648 - 648
  • [9] New c-terminal titin mutations in Europeans with tibial muscular dystrophy (TMD)
    Hackman, P.
    Marchand, S.
    Penisson-Besnier, I.
    Hammouda, E.
    Illa, I.
    Eymard, B.
    Pardal-Fenandez, J.
    Richard, I.
    Udd, B.
    NEUROMUSCULAR DISORDERS, 2007, 17 (9-10) : 884 - 884
  • [10] Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42
    Brockington, M
    Sewry, CA
    Herrmann, R
    Naom, I
    Dearlove, A
    Rhodes, M
    Topaloglu, H
    Dubowitz, V
    Voit, T
    Muntoni, F
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (02) : 428 - 435