Mutation analysis of two candidate genes in the paroxysmal dystonic choreoathetosis locus on chromosome 2q.

被引:0
|
作者
Tokarz, D [1 ]
Thomas, D [1 ]
Rainier, SR [1 ]
Fink, JK [1 ]
机构
[1] Univ Michigan, Dept Neurol, Ann Arbor, MI USA
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
2633
引用
收藏
页码:629 / 629
页数:1
相关论文
共 50 条
  • [1] Analysis of nine candidate genes for autism on chromosome 2q.
    Maestrini, E
    Bacchelli, E
    Blasi, F
    Biondolillo, M
    Bailey, AJ
    Monaco, AP
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 497 - 497
  • [2] Paroxysmal dystonic choreoathetosis: Tight linkage to chromosome 2q
    Fink, JK
    Rainier, S
    Wilkowski, J
    Jones, SM
    Kume, A
    Hedera, P
    Albin, R
    Mathay, J
    Girbach, L
    Varvil, T
    Otterud, B
    Leppert, M
    AMERICAN JOURNAL OF HUMAN GENETICS, 1996, 59 (01) : 140 - 145
  • [3] Paroxysmal dystonic choreoathetosis linked to chromosome 2q: Clinical analysis and proposed pathophysiology
    Fink, JK
    Hedera, P
    Mathay, JG
    Albin, RL
    NEUROLOGY, 1997, 49 (01) : 177 - 183
  • [4] Mutational analysis of the anion exchanger 3 gene in familial paroxysmal dystonic choreoathetosis linked to chromosome 2q
    Matsuo, H
    Kamakura, K
    Matsushita, S
    Ohmori, T
    Okano, M
    Tadano, Y
    Tsuji, S
    Higuchi, S
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1999, 88 (06): : 733 - 737
  • [5] Mutation analysis of two candidate genes within the hereditary neuralgic amyotrophy locus on chromosome 17q25.
    Watts, GDJ
    Keller, MP
    Iismaa, TP
    Chance, PF
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A498 - A498
  • [6] Further localization of a gene for paroxysmal dystonic choreoathetosis to a 5-cM region on chromosome 2q34
    Raskind, WH
    Bolin, T
    Wolff, J
    Fink, J
    Matsushita, M
    Litt, M
    Lipe, H
    Bird, TD
    HUMAN GENETICS, 1998, 102 (01) : 93 - 97
  • [7] Further localization of a gene for paroxysmal dystonic choreoathetosis to a 5-cM region on chromosome 2q34
    W. H. Raskind
    Tamara Bolin
    John Wolff
    John Fink
    Mark Matsushita
    Michael Litt
    Hillary Lipe
    Thomas D. Bird
    Human Genetics, 1998, 102 : 93 - 97
  • [8] Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1
    Tomita, H
    Nagamitsu, S
    Wakui, K
    Fukushima, Y
    Yamada, K
    Sadamatsu, M
    Masui, A
    Konishi, T
    Matsuishi, T
    Aihara, M
    Shimizu, K
    Hashimoto, K
    Mineta, M
    Matsushima, M
    Tsujita, T
    Saito, M
    Tanaka, H
    Tsuji, S
    Takagi, T
    Nakamura, Y
    Nanko, S
    Kato, N
    Nakane, Y
    Niikawa, N
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (06) : 1688 - 1697
  • [9] Mutation screening in a family with "coralliform" cataract that maps to chromosome 2q.
    Francis, PJ
    Berry, V
    Moore, A
    Bhattacharya, SS
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2000, 41 (04) : S1 - S1
  • [10] A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16
    Valente, EM
    Spacey, SD
    Wali, GM
    Bhatia, KP
    Dixon, PH
    Wood, NW
    Davis, MB
    BRAIN, 2000, 123 : 2040 - 2045