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
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