A novel form of autosomal dominant pure spastic paraplegia (SP) maps to chromosome 12q23-24

被引：0
|
作者：
Schule, Rebecca
Durr, Alexandra
Kassubek, Jan
Klimpe, Sven
Van De Warrenburg, B. P. C.
Schoels, Ludger
机构：
来源：
NEUROLOGY | 2007年 / 68卷 / 12期
关键词：
D O I：
暂无
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：A252 / A252
页数：1
相关论文
共 50 条
  • [41] Increased intracortical facilitation in patients with autosomal dominant pure spastic paraplegia linked to chromosome 2p
    Nielsen, JE
    Jennum, P
    Fenger, K
    Sorensen, SA
    Fuglsang-Frederiksen, A
    EUROPEAN JOURNAL OF NEUROLOGY, 2001, 8 (04) : 335 - 339
  • [42] MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia
    Selcuk, Ece
    Kirimtay, Koray
    Temizci, Benan
    Akarsu, Seyma
    Everest, Elif
    Baslo, Mehmet Baris
    Demirkiran, Meltem
    Yapici, Zuhal
    Karabay, Arzu
    MOLECULAR GENETICS AND GENOMICS, 2022, 297 (04) : 1141 - 1150
  • [43] MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia
    Ece Selçuk
    Koray Kırımtay
    Benan Temizci
    Şeyma Akarsu
    Elif Everest
    Mehmet Barış Baslo
    Meltem Demirkıran
    Zuhal Yapıcı
    Arzu Karabay
    Molecular Genetics and Genomics, 2022, 297 : 1141 - 1150
  • [44] A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia
    Rydning, S. L.
    Dudesek, A.
    Rimmele, F.
    Funke, C.
    Krueger, S.
    Biskup, S.
    Vigeland, M. D.
    Hjorthaug, H. S.
    Sejersted, Y.
    Tallaksen, C.
    Selmer, K. K.
    Kamm, C.
    EUROPEAN JOURNAL OF NEUROLOGY, 2018, 25 (07) : 943 - +
  • [45] A novel locus for autosomal dominant familial aortic aneurysm maps to human chromosome 11q23
    Vaughan, CJ
    Casey, M
    Roman, MJ
    Campagna, R
    Basson, CT
    CIRCULATION, 2000, 102 (18) : 163 - 163
  • [46] The gene for HMSN2C maps to 12q23-24 - A region of neuromuscular disorders
    Klein, CJ
    Cunningham, JM
    Atkinson, EJ
    Schaid, DJ
    Hebbring, SJ
    Anderson, SA
    Klein, DM
    Dyck, PJB
    Litchy, WJ
    Thibodeau, SN
    NEUROLOGY, 2003, 60 (07) : 1151 - 1156
  • [47] A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qter
    Blanton, SH
    Liang, CY
    Cai, MW
    Pandya, A
    Du, LL
    Landa, B
    Mummalanni, S
    Li, KS
    Chen, ZY
    Qin, XN
    Liu, YF
    Balkany, T
    Nance, WE
    Liu, XZ
    JOURNAL OF MEDICAL GENETICS, 2002, 39 (08) : 567 - 570
  • [48] A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qter.
    Liu, XZ
    Blanton, SH
    Liang, CY
    Cai, MW
    Pandya, A
    Landa, B
    Mummalanni, S
    Li, KS
    Du, LL
    Qin, XN
    Liu, YF
    Nance, WE
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 495 - 495
  • [49] A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1-12q14
    Wilkinson, PA
    Simpson, MA
    Bastaki, L
    Patel, H
    Reed, JA
    Kalidas, K
    Samilchuk, E
    Khan, R
    Warner, TT
    Crosby, AH
    JOURNAL OF MEDICAL GENETICS, 2005, 42 (01) : 80 - 82
  • [50] A new autosomal dominant pure cerebellar ataxia - Maps to chromosome 4q34.3-q35.1
    Storey, Elsdon
    Sisson, Oliver
    Fahey, Michael C.
    Lueck, Christian J.
    Bahlo, Melanie
    Gardner, R. J. McKinlay
    NEUROLOGY, 2008, 70 (11) : A316 - A316
12345