作者：
Haack,T.B. [1]
;
Gorza,M. [2]
;
Danhauser,K. [3]
;
Mayr,J.A. [4]
;
Haberberger,B. [5]
;
Wieland,T. [6]
;
Kremer,L. [7]
;
Strecker,V. [8]
;
Graf,E. [9]
;
Memari,Y. [10]
;
Ahting,U. [11]
;
Kopajtich,R. [12]
;
Wortmann,S.B. [13]
;
Rodenburg,R.J. ;
Kotzaeridou,U. ;
Hoffmann,G.F. ;
Sperl,W. ;
Wittig,I. ;
Wilichowski,E. ;
Schottmann,G. ;
Schuelke,M. ;
Plecko,B. ;
Stephani,U. ;
Strom,T.M. ;
Meitinger,T. ;
Prokisch,H. ;
Freisinger,P.
作者单位：
Department of Pediatrics, Inherited Metabolic Disease Centre, Klinikum Reutlingen, 72764 Reutlingen
[1]
Institute of Human Genetics, Technische Universit?t München, 81675 Munich, Germany
[2]
Department of Pediatrics and Pediatric Neurology, Universit?tsmedizin G?ttingen, 37075 G?ttingen
[3]
Institute of Human Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany
[4]
Institute of Human Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany, Institute of
[5]
Department of General Pediatrics, Division of Inherited Metabolic Diseases, University Children's
[6]
Functional Proteomics, Faculty of Medicine, Goethe-University, SFB 815 core unit, 60590 Frankfurt
[7]
Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, United Kingdom
[8]
Department of Neurology, Kinderspital Zürich, Zürich, Switzerland
[9]
Nijmegen Center for Mitochondrial Disorders, Department of Pediatrics, Radboud University Nijmegen
[10]
Department of Neuropediatrics, University Hospital, 24105 Kiel, Germany
[11]
Department of Pediatrics, Paracelsus Medical University Salzburg, 5020 Salzburg, Austria
[12]
Department of Neuropediatrics and NeuroCure Clinical Research Center, Charité Universit?tsmedizin
[13]
发布时间
2014-06-29
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