Gene therapy for Dopamine transporter deficiency syndrome: Infantile Parkinsonism-dystonia

被引:0
|
作者
Ng, J. [1 ]
Barral, S. [1 ]
Barrigon, C. de la Fuente [1 ]
Lignani, G. [1 ]
Erdem, F. [1 ,2 ]
Wallings, R. [3 ]
Privolizzi, R. [1 ]
Rossignoli, G. [1 ]
Al Rashidi, H. [1 ]
Heasman, S. [1 ]
Meyer, E. [1 ]
Ngoh, A. [1 ]
Pope, S.
Karda, R. [1 ]
Perocheau, D. [1 ]
Baruteau, J. [1 ,6 ]
Suff, N. [1 ,4 ]
Diaz, J. A. Antinao [1 ]
Vowles, J. [3 ]
Cowley, S. A. [1 ]
Friessmuth, M. [2 ]
Sucic, S. [2 ]
Counsell, J. [1 ]
Wade-Martins, R. [3 ]
Heales, S. J. R. [5 ,6 ]
Rahim, A. A. [1 ]
Bencze, M. [1 ]
Waddington, S. N. [1 ]
Kurian, M. A. [1 ,6 ]
机构
[1] UCL, London, England
[2] Med Univ Vienna, Vienna, Austria
[3] Univ Oxford, Oxford, England
[4] Kings Coll London, London, England
[5] Natl Hosp Neurol & Neurosurg, London, England
[6] Great Ormond St Hosp Sick Children, London, England
关键词
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
P070
引用
收藏
页码:A50 / A50
页数:1
相关论文
共 50 条
  • [1] Infantile parkinsonism-dystonia: a dopamine "transportopathy"
    Blackstone, Craig
    JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (06): : 1455 - 1458
  • [2] Infantile parkinsonism-dystonia due to dopamine transporter gene mutations: another genetic twist
    Blackstone, Craig
    LANCET NEUROLOGY, 2011, 10 (01): : 24 - 25
  • [3] Infantile Parkinsonism-dystonia: Tyrosine hydroxylase deficiency
    Surtees, R
    Clayton, P
    MOVEMENT DISORDERS, 1998, 13 (02) : 350 - 350
  • [4] Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia
    Kurian, Manju A.
    Zhen, Juan
    Cheng, Shu-Yuan
    Li, Yan
    Mordekar, Santosh R.
    Jardine, Philip
    Morgan, Neil V.
    Meyer, Esther
    Tee, Louise
    Pasha, Shanaz
    Wassmer, Evangeline
    Heales, Simon J. R.
    Gissen, Paul
    Reith, Maarten E. A.
    Maher, Eamonn R.
    JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (06): : 1595 - 1603
  • [5] Infantile parkinsonism-dystonia and elevated dopamine metabolites in CSF
    Assmann, BE
    Robinson, RO
    Surtees, RAH
    Bräutigam, C
    Heales, SJR
    Wevers, RA
    Zschocke, J
    Hyland, K
    Sharma, R
    Hoffmann, GF
    NEUROLOGY, 2004, 62 (10) : 1872 - 1874
  • [6] Modeling infantile Parkinsonism-Dystonia in flies
    Le Bras, Alexandra
    LAB ANIMAL, 2021, 50 (07) : 166 - 166
  • [7] Molybdenum cofactor deficiency presenting with a parkinsonism-dystonia syndrome
    Alkufri, Fadi
    Harrower, Tim
    Rahman, Yusof
    Hughes, Elaine
    Mundy, Helen
    Knibb, Jonathan A.
    Moriarty, John
    Connor, Stephen
    Samuel, Michael
    MOVEMENT DISORDERS, 2013, 28 (03) : 399 - 400
  • [8] Modeling infantile Parkinsonism-Dystonia in flies
    Alexandra Le Bras
    Lab Animal, 2021, 50 : 166 - 166
  • [9] PARKINSONISM-DYSTONIA SYNDROME AND ECT
    LAUTERBACH, EC
    MOORE, NC
    AMERICAN JOURNAL OF PSYCHIATRY, 1990, 147 (09): : 1249 - 1250
  • [10] A specific subtype of Infantile Parkinsonism-dystonia identified
    Fisher, E.
    CLINICAL GENETICS, 2011, 79 (04) : 332 - 334