Identifying the disease-causing variant in a large family, with a late-onset dominant distal myopathy

被引:0
|
作者
Turku, T. [1 ]
Savarese, M. [1 ]
Johari, M. [1 ,2 ]
Soininen, M. [1 ]
Hoischen, A. [3 ,4 ,5 ]
Steehouwer, M. [3 ]
Roos, A. [6 ,7 ]
Preusse, C. [8 ,9 ,10 ,11 ,12 ]
Stenzel, W. [8 ,9 ,10 ,11 ]
Wallgren-Pettersson, C. [1 ]
Pelin, K. [1 ]
Udd, B. [1 ]
Hackman, P. [1 ]
机构
[1] Folkhalsan Res Ctr, Helsinki, Finland
[2] Univ Western Australia, Harry Perkins Inst Med Res, Ctr Med Res, Nedlands, WA, Australia
[3] Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands
[4] Radboud Univ Nijmegen, Med Ctr, Radboud Expertise Ctr Immunodeficiency & Autoinfl, Dept Internal Med,Radboud Inst Mol Life Sci, Nijmegen, Netherlands
[5] Radboud Univ Nijmegen, Med Ctr, Radboud Ctr Infect Dis RCI, Nijmegen, Netherlands
[6] Univ Duisburg Essen, Univ Childrens Hosp, Pediat Neurol, Fac Med, Essen, Germany
[7] Univ Ottawa, Childrens Hosp Eastern Ontario, Res Inst, Ottawa, ON, Canada
[8] Charite Univ Med Berlin, Dept Neuropathol, Berlin, Germany
[9] Free Univ Berlin, Berlin, Germany
[10] Humboldt Univ, Berlin, Germany
[11] Berlin Inst Hlth, Berlin, Germany
[12] Charite Univ Med Berlin, Dept Neuropediat, Berlin, Germany
关键词
D O I
10.1016/j.nmd.2024.07.426
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
63P
引用
收藏
页数:2
相关论文
共 50 条
  • [31] HISTOCHEMICAL AND HISTOPATHOLOGICAL CHANGES IN SKELETAL-MUSCLE IN LATE-ONSET HEREDITARY DISTAL MYOPATHY (WELANDER)
    EDSTROM, L
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 1975, 26 (02) : 147 - 157
  • [32] Novel disease-causing variant in RDH12 presenting with autosomal dominant retinitis pigmentosa
    Muthiah, Manickam Nick
    Kalitzeos, Angelos
    Oprych, Kate
    Singh, Navjit
    Georgiou, Michalis
    Wright, Genevieve Ann
    Robson, Anthony G.
    Arno, Gavin
    Khan, Kamron
    Michaelides, Michel
    BRITISH JOURNAL OF OPHTHALMOLOGY, 2022, 106 (09) : 1274 - 1281
  • [33] Molecular Genetic Analysis of Autosomal Dominant Late-Onset Cataract in a Chinese Family
    Yang, Guohua
    Zhong, Shan
    Zhang, Xianrong
    Peng, Biwen
    Li, Jun
    Ke, Tie
    Xu, Hua
    JOURNAL OF HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY-MEDICAL SCIENCES, 2010, 30 (06) : 792 - 797
  • [34] ''Pure'' autosomal dominant spastic paraplegia with late-onset dementia: A family study
    Webb, S
    Coleman, D
    Hutchinson, J
    Hutchinson, M
    ANNALS OF NEUROLOGY, 1996, 40 (03) : T159 - T159
  • [35] Autosomal dominant late-onset leukoencephalopathy - Clinical report of a new Italian family
    Quattrocolo, G
    Leombruni, S
    Vaula, G
    Bergui, M
    Riva, A
    Bradac, GB
    Bergamini, L
    EUROPEAN NEUROLOGY, 1997, 37 (01) : 53 - 61
  • [36] Molecular genetic analysis of autosomal dominant late-onset cataract in a Chinese Family
    Guohua Yang
    Shan Zhong
    Xianrong Zhang
    Biwen Peng
    Jun Li
    Tie Ke
    Hua Xu
    Journal of Huazhong University of Science and Technology [Medical Sciences], 2010, 30 : 792 - 797
  • [37] Are Late-Onset Autosomal Dominant and Sporadic Alzheimer Disease "Separate but Equal"?
    Ringman, John M.
    JAMA NEUROLOGY, 2016, 73 (09) : 1060 - 1061
  • [38] Alexander disease causing hereditary, late-onset ataxia in two sibs
    Delnooz, C. C. S.
    de Graaf, R. J.
    Salomons, G. S.
    Schelhaas, H. J.
    van de Warrenburg, B. P. C.
    MOVEMENT DISORDERS, 2008, 23 (01) : S151 - S151
  • [39] A novel glycogenin-1 gene mutation in a family with late-onset proximal myopathy
    Angelini, Corrado
    Fanin, Marina
    Nigro, Vincenzo
    Torella, Annalaura
    Savarese, Marco
    NEUROLOGY, 2016, 86
  • [40] A Novel Late-onset Dominant Episodic Ataxia in a Large French Canadian Kindred
    Pellerin, David
    Renaud, Mathilde
    Choquet, Karine
    Tetreault, Martine
    Provost, Sylvie
    Dicaire, Marie-Josee
    La Piana, Roberta
    Massie, Rami
    Chalk, Colin
    Lafontaine, Anne-Louise
    Dube, Marie-Pierre
    Duquette, Antoine
    Brais, Bernard
    NEUROLOGY, 2020, 94 (15)