Studies of the CAG repeat in the spinocerebellar ataxia type 7 gene in Taiwan.

被引：0
|
作者：
Hsieh, M
Lin, SJ
Chen, JF
Lin, HM
Hsiao, KM
Li, C
Li, SY
机构：
[1] Chung Shan Med & Dent Coll, Inst Med, Taichung, Taiwan
[2] Chung Shan Med & Dent Coll, Sch Med Technol, Taichung, Taiwan
[3] Chung Shan Med & Dent Coll, Dept Life Sci, Taichung, Taiwan
[4] Natl Cheng Kung Univ, Dept Pediat, Tainan 70101, Taiwan
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1999年 / 65卷 / 04期
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：
1535
引用
收藏
页码：A275 / A275
页数：1
相关论文
共 50 条
  • [21] A NOVEL CAG REPEAT CONFIGURATION IN THE SCA1 GENE - IMPLICATIONS FOR THE MOLECULAR DIAGNOSTICS OF SPINOCEREBELLAR ATAXIA TYPE-1
    QUAN, F
    JANAS, J
    POPOVICH, BW
    HUMAN MOLECULAR GENETICS, 1995, 4 (12) : 2411 - 2413
  • [22] CAG repeat expansion in α1A-voltage-dependent calcium channel gene and clinical variations in spinocerebellar ataxia type 6
    Ikeuchi, T
    Takano, H
    Koide, R
    Horikawa, Y
    Honma, Y
    Onishi, Y
    Igarashi, S
    Tanaka, H
    Nakao, N
    Sahashi, K
    Tsukagoshi, H
    Inoue, K
    Takahashi, H
    Tsuji, S
    AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : A311 - A311
  • [23] Intergenerational instability and genetic flow of the CAG repeat at the ATXN2 gene in Cuban families with spinocerebellar ataxia type 2
    Almaguer-Mederos, L. E.
    Gonzalez-Zaldivar, Y.
    Almaguer-Gotay, D.
    Laffita-Mesa, J. M.
    Mejias-Brito, S.
    Cuello-Almarales, D.
    MOVEMENT DISORDERS, 2012, 27 : S447 - S447
  • [24] CAG repeat mosaicism is gene specific in spinocerebellar ataxias
    Kacher, Radhia
    Lejeune, Francois-Xavier
    David, Isabelle
    Boluda, Susana
    Coarelli, Giulia
    Leclere-Turbant, Sabrina
    Heinzmann, Anna
    Marelli, Cecilia
    Charles, Perrine
    Goizet, Cyril
    Kabir, Nisha
    Hilab, Rania
    Jornea, Ludmila
    Six, Julie
    Dommergues, Marc
    Fauret, Anne-Laure
    Brice, Alexis
    Humbert, Sandrine
    Durr, Alexandra
    AMERICAN JOURNAL OF HUMAN GENETICS, 2024, 111 (05) : 913 - 926
  • [25] Association between a CAG repeat polymorphism in the hKCa3 channel gene and spinocerebellar ataxia (SCA).
    Figueroa, K
    Geshwind, D
    Perlman, S
    Chan, P
    Tanner, C
    Pulst, S
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A249 - A249
  • [26] Somatic mosaicism of the CAG repeat expansion in spinocerebellar ataxia type 3 Machado-Joseph disease
    Cancel, G
    Gourfinkel-An, I
    Stevanin, G
    Didierjean, O
    Abbas, N
    Hirsch, E
    Agid, Y
    Brice, A
    HUMAN MUTATION, 1998, 11 (01) : 23 - 27
  • [27] Redefining the Pathogenic CAG Repeat Units Threshold in CACNA1A for Spinocerebellar Ataxia Type 6
    Hatano, Yuya
    Ishihara, Tomohiko
    Hirokawa, Sachiko
    Date, Hidetoshi
    Takahashi, Yuji
    Mizusawa, Hidehiro
    Onodera, Osamu
    NEUROLOGY-GENETICS, 2025, 11 (02)
  • [28] Molecular analysis of the CAG repeat among patients with Type-2 spinocerebellar ataxia in the Mexican population
    Magana, Jonathan J.
    Dolores Vergara, Maria
    Sierra-Martinez, Monica
    Garcia-Jimenez, Elvia
    Rodriguez-Antonio, Facundo
    del Rocio Gomez, Maria
    Valdes-Flores, Margarita
    Cisneros, Bulmaro
    GACETA MEDICA DE MEXICO, 2008, 144 (05): : 413 - 418
  • [29] Spinocerebellar Ataxia Type 2: CAG Repeat Expansion Size of ATXN2 in the Pediatric Population
    Stanley, Christine M.
    Hill, David
    Casey, Kristie
    Bishop, Crystal
    Moore, Rebecca
    Ito, Masamichi
    NEUROLOGY, 2011, 76 (09) : A350 - A350
  • [30] Hypothalamic Atrophy, Expanded CAG Repeat, and Low Body Mass Index in Spinocerebellar Ataxia Type 3
    Guo, Jing
    Jiang, Zhouyu
    Biswal, Bharat B.
    Zhou, Bo
    Xie, Dongjing
    Gao, Qing
    Sheng, Wei
    Chen, Hui
    Zhang, Yuhan
    Fan, Yunshuang
    Wang, Jian
    Liu, Chen
    Chen, Huafu
    MOVEMENT DISORDERS, 2022, 37 (07) : 1541 - 1546
12345