HOMOZYGOSITY FOR THE TRANSTHYRETIN-MET30-GENE IN 2 SWEDISH SIBS WITH FAMILIAL AMYLOIDOTIC POLYNEUROPATHY

被引:0
|
作者
HOLMGREN, G
HAETTNER, E
NORDENSON, I
SANDGREN, O
STEEN, L
LUNDGREN, E
机构
[1] UMEA UNIV HOSP,DEPT INTERNAL MED,APPL MOLEC BIOL UNIT,S-90185 UMEA,SWEDEN
[2] UMEA UNIV HOSP,DEPT OPHTHALMOL,S-90185 UMEA,SWEDEN
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
引用
收藏
页码:333 / 338
页数:6
相关论文
共 50 条
  • [1] HOMOZYGOSITY FOR THE MET30 TRANSTHYRETIN GENE IN A TURKISH KINDRED WITH FAMILIAL AMYLOIDOTIC POLYNEUROPATHY
    SKARE, J
    YAZICI, H
    ERKEN, E
    DEDE, H
    COHEN, A
    MILUNSKY, A
    SKINNER, M
    HUMAN GENETICS, 1990, 86 (01) : 89 - 90
  • [2] HOMOZYGOSITY FOR THE TRANSTHYRETIN-MET30 GENE IN 3 JAPANESE SIBLINGS WITH TYPE-I FAMILIAL AMYLOIDOTIC POLYNEUROPATHY
    YOSHINAGA, T
    NAKAZATO, M
    IKEDA, S
    OHNISHI, A
    NEUROLOGY, 1992, 42 (10) : 2045 - 2047
  • [3] DIAGNOSTIC RADIOIMMUNOASSAY AND DNA-ANALYSIS IN SWEDISH AND JAPANESE PATIENTS WITH FAMILIAL AMYLOIDOTIC POLYNEUROPATHY - HOMOZYGOSITY FOR THE TTR MET30 GENE
    HOLMGREN, G
    LUNDGREN, E
    KANGAWA, K
    KURIHARA, T
    MATSUKURA, S
    MATSUO, H
    NAKAZATO, M
    STEEN, L
    ACTA NEUROLOGICA SCANDINAVICA, 1993, 87 (02): : 124 - 127
  • [4] HOMOZYGOSITY FOR THE TRANSTHYRETIN-MET30-GENE IN 7 INDIVIDUALS WITH FAMILIAL AMYLOIDOSIS WITH POLYNEUROPATHY DETECTED BY RESTRICTION ENZYME ANALYSIS OF AMPLIFIED GENOMIC DNA-SEQUENCES
    HOLMGREN, G
    BERGSTROM, S
    DRUGGE, U
    LUNDGREN, E
    NORDINGSIKSTROM, C
    SANDGREN, O
    STEEN, L
    CLINICAL GENETICS, 1992, 41 (01) : 39 - 41
  • [5] MOLECULAR DIAGNOSIS OF TRANSTHYRETIN MET(30) MUTATION IN AN ITALIAN FAMILY WITH FAMILIAL AMYLOIDOTIC POLYNEUROPATHY
    STROCCHI, P
    TANG, XM
    CAMBI, F
    FEBS LETTERS, 1995, 359 (2-3): : 203 - 205
  • [6] TRANSTHYRETIN AND FAMILIAL AMYLOIDOTIC POLYNEUROPATHY
    ANDO, Y
    ARAKI, S
    ANDO, M
    INTERNAL MEDICINE, 1993, 32 (12) : 920 - 920
  • [7] Postmortem findings in a familial amyloid polyneuropathy patient with homozygosity of the mutant Val30Met transthyretin gene
    Yoshinaga, T
    Takei, YI
    Katayanagi, K
    Ikeda, SI
    AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2004, 11 (01): : 56 - 60
  • [8] Continuous Development of Arrhythmia Is Observed in Swedish Transplant Patients With Familial Amyloidotic Polyneuropathy (Amyloidogenic Transthyretin Val30Met Variant)
    Okamoto, Sadahisa
    Hoernsten, Rolf
    Obayashi, Konen
    Wijayatunga, Priyantha
    Suhr, Ole B.
    LIVER TRANSPLANTATION, 2011, 17 (02) : 122 - 128
  • [9] Effect of albumin on transthyretin and amyloidogenic transthyretin Val30Met disposition and tissue deposition in familial amyloidotic polyneuropathy
    Taguchi, Kazuaki
    Jono, Hirofumi
    Kugimiya-Taguchi, Tomoe
    Nagao, Saori
    Su, Yu
    Yamasaki, Keishi
    Mizuguchi, Mineyuki
    Maruyama, Toru
    Ando, Yukio
    Otagiri, Masaki
    LIFE SCIENCES, 2013, 93 (25-26) : 1017 - 1022
  • [10] Frequency of arrhythmia in Swedish familial amyloidotic polyneuropathy (ATTR Val30Met) transplanted
    Okamoto, S.
    Hornsten, R.
    Suhr, O. B.
    AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2010, 17 : 137 - 137