作者：
Burcu,Ayoglu [1]
;
Amina,Chaouch [2]
;
Hanns,Lochmüller [2]
;
Luisa,Politano [3]
;
Enrico,Bertini [4]
;
Pietro,Spitali [5]
;
Monika,Hiller [5]
;
Eric H,Niks [6]
;
Francesca,Gualandi [7]
;
Fredrik,Pontén [8]
;
Kate,Bushby [2]
;
Annemieke,Aartsma-Rus [9]
;
Elena,Schwartz [10]
;
Yannick,Le Priol [11]
;
Volker,Straub [2]
;
Mathias,Uhlén [1]
;
Sebahattin,Cirak [12]
;
Peter A C,'t Hoen [5]
;
Francesco,Muntoni [13]
;
Alessandra,Ferlini [7]
;
Jochen M,Schwenk [1]
;
Peter,Nilsson [1]
;
Cristina,Al-Khalili Szigyarto [14]
作者单位：
Affinity Proteomics, SciLifeLab, School of Biotechnology KTH-Royal Institute of Technology, Stockholm, Sweden.
[1]
Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.
[2]
Cardiomiology and Medical Genetics, Department of Experimental Medicine, Second University of Naples, Naples, Italy.
[3]
Unit of Neuromuscular and Neurodegenerative Disorders, Department of Neurosciences, Bambino Gesú Children's Hospital, Rome, Italy.
[4]
Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
[5]
Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
[6]
Unit of Medical Genetics, Department of Medical Sciences, University of Ferrara, Ferrara, Italy.
[7]
SciLifeLab, Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
[8]
Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
[9]
Ariadne Diagnostics, Rockville, MD, USA.
[10]
Elsevier, Amsterdam, The Netherlands.
[11]
Research Center for Genetic Medicine, Childrens National Medical Center, Washington, DC, USA.
[12]
The Dubowitz Neuromuscular Centre, UCL Institute of Child Health, London, UK.
[13]
Department of Proteomics, School of Biotechnology KTH-Royal Institute of Technology, Stockholm, Sweden caks@kth.se.
[14]
DOI
10.15252/emmm.201303724
PMID
24920607
发布时间
2022-01-29
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