43rd ENMC International Workshop on Emery-Dreifuss Muscular Dystrophy, 22 June 1996, Naarden, The Netherlands

被引:23
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Yates, JRW
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10.1016/S0960-8966(96)00403-8
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R74 [神经病学与精神病学];
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页码:67 / 69
页数:3
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  • [1] BIONE S, 1995, HUM MOL GENET, V4, P1859
  • [2] IDENTIFICATION OF A NOVEL X-LINKED GENE RESPONSIBLE FOR EMERY-DREIFUSS MUSCULAR-DYSTROPHY
    BIONE, S
    MAESTRINI, E
    RIVELLA, S
    MANCINI, M
    REGIS, S
    ROMEO, G
    TONIOLO, D
    [J]. NATURE GENETICS, 1994, 8 (04) : 323 - 327
  • [3] Emery AE, 1993, DUCHENNE MUSCULAR DY
  • [4] EMERY-DREIFUSS SYNDROME
    EMERY, AEH
    [J]. JOURNAL OF MEDICAL GENETICS, 1989, 26 (10) : 637 - 641
  • [5] IDENTIFICATION OF NOVEL MUTATIONS IN 3 FAMILIES WITH EMERY-DREIFUSS MUSCULAR-DYSTROPHY
    KLAUCK, SM
    WILGENBUS, P
    YATES, JRW
    MULLER, CR
    POUSTKA, A
    [J]. HUMAN MOLECULAR GENETICS, 1995, 4 (10) : 1853 - 1857
  • [6] The Emery-Dreifuss muscular dystrophy protein, emerin, is a nuclear membrane protein
    Manilal, S
    Man, NT
    Sewry, CA
    Morris, GE
    [J]. HUMAN MOLECULAR GENETICS, 1996, 5 (06) : 801 - 808
  • [7] McKusick VA, 1990, MENDELIAN INHERITANC
  • [8] Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophy
    Nagano, A
    Koga, R
    Ogawa, M
    Kurano, Y
    Kawada, J
    Okada, R
    Hayashi, YK
    Tsukahara, T
    Arahata, K
    [J]. NATURE GENETICS, 1996, 12 (03) : 254 - 259
  • [9] SSCP DETECTION OF NOVEL MUTATIONS IN PATIENTS WITH EMERY-DREIFUSS MUSCULAR-DYSTROPHY - DEFINITION OF A SMALL C-TERMINAL REGION REQUIRED FOR EMERIN FUNCTION
    NIGRO, V
    BRUNI, P
    CICCODICOLA, A
    POLITANO, L
    NIGRO, G
    PILUSO, G
    CAPPA, V
    COVONE, AE
    ROMEO, G
    DURSO, M
    [J]. HUMAN MOLECULAR GENETICS, 1995, 4 (10) : 2003 - 2004
  • [10] A novel emerin mutation in a Japanese patient with Emery-Dreifuss muscular dystrophy
    Yamada, T
    Kobayashi, T
    [J]. HUMAN GENETICS, 1996, 97 (05) : 693 - 694