LINKAGE DISEQUILIBRIUM BETWEEN SPINOCEREBELLAR ATAXIA (SCA1) AND D6S89 LOCI

被引：0
|
作者：
TERRENATO, L
JODICE, C
MALASPINA, P
NOVELLETTO, A
PERSICHETTI, F
SCHINAIA, G
FRONTALI, M
LULLI, P
CAPPELLACCI, S
GIUNTI, P
SPADARO, M
ANTONELLI, A
PANDOLFO, M
机构：
[1] UNIV TOR VERGATA ROME,DIP BIOL,ROME,ITALY
[2] UNIV ROMA LA SAPIENZA,IST CLIN MALATTIE NERV & MENT,I-00185 ROME,ITALY
[3] IST NEUROCHIRURG C BESTA,I-20133 MILAN,ITALY
[4] CNR,DIP MED SPERIM,ROME,ITALY
来源：
CYTOGENETICS AND CELL GENETICS | 1993年 / 62卷 / 2-3期
关键词：
D O I：
暂无
中图分类号：
Q2 [细胞生物学];
学科分类号：
071009 ; 090102 ;
摘要：
引用
收藏
页码：80 / 80
页数：1
相关论文
共 50 条
  • [31] Cognition in Patients with Spinocerebellar Ataxia 1 (SCA1) and 2 (SCA2): A Neurophysiological and Neuropsychological Approach
    Colucci, Fabiana
    Stefanelli, Sara
    Contaldi, Elena
    Gozzi, Andrea
    Marchetti, Alessia
    Pugliatti, Maura
    Laudisi, Michele
    Antenucci, Pietro
    Capone, Jay Guido
    Gragnaniello, Daniela
    Sensi, Mariachiara
    JOURNAL OF CLINICAL MEDICINE, 2024, 13 (16)
  • [32] Normal variation in SCA1 and SCA6 CAG repeats modifies age of onset in spinocerebellar ataxia type 2 (SCA2)
    Figueroa, KP
    Santos, N
    Velazquez, L
    Pulst, SM
    NEUROLOGY, 2002, 58 (07) : A16 - A16
  • [33] Spinocerebellar ataxia type 1 (SCA1): new pathoanatomical and clinico-pathological insights
    Rueb, U.
    Buerk, K.
    Timmann, D.
    den Dunnen, W.
    Seidel, K.
    Farrag, K.
    Brunt, E.
    Heinsen, H.
    Egensperger, R.
    Bornemann, A.
    Schwarzacher, S.
    Korf, H. -W.
    Schoels, L.
    Bohl, J.
    Deller, T.
    NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 2012, 38 (07) : 665 - 680
  • [34] Trinucleotide repeat polymorphisms of Spinocerebellar ataxia type 1 gene (SCA1) in Asian populations
    Yee, Su-Bog
    Lee, Su Hun
    Shim, Ji Young
    Kim, Nam Deuk
    KOREAN JOURNAL OF GENETICS, 2007, 29 (01): : 21 - 28
  • [35] Clinico-genetic correlation in Indian Spinocerebellar ataxia Type 1 (SCA1) patients
    Takkar, A.
    Ahmed, I.
    Shakya, S.
    Srivastava, A.
    MOVEMENT DISORDERS, 2018, 33 : S293 - S293
  • [36] CLINICO-GENETIC CORRELATION IN INDIAN SPINOCEREBELLAR ATAXIA TYPE 1 (SCA1) PATIENTS
    Takkar, A.
    Srivastava, A.
    Faruq, M.
    PARKINSONISM & RELATED DISORDERS, 2018, 46 : E4 - E4
  • [37] Evaluating the effects of deep brain stimulation (DBS) in mice with spinocerebellar ataxia (SCA1)
    Vedam-Mai, V.
    McFarland, K.
    Zhang, Q.
    Kim, H.
    Nathu, R.
    Kurtovic, S.
    Savery, K.
    Ashizawa, T.
    Okun, M. S.
    MOVEMENT DISORDERS, 2016, 31 : S345 - S345
  • [38] Spinocerebellar ataxia type I (SCA1): Revised diagnosis of a familial multiple sclerosis
    Kreuz, FR
    Deike, H
    AKTUELLE NEUROLOGIE, 1999, 26 (08) : 375 - 378
  • [39] Pseudo-Argyll Robertson pupil of patients with spinocerebellar ataxia type 1(SCA1)
    Mabuchi, K
    Yoshikawa, H
    Takamori, M
    Yokoji, H
    Takahira, M
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1998, 65 (04): : 612 - 613
  • [40] The effect of CAT trinucleotide interruptions on the age at onset of spinocerebellar ataxia type 1 (SCA1)
    Matsuyama, Z
    Izumi, Y
    Kameyama, M
    Kawakami, H
    Nakamura, S
    JOURNAL OF MEDICAL GENETICS, 1999, 36 (07) : 546 - 548
12345