作者：
Campeau,P.M. [1]
;
Lenk,G.M. [2]
;
Lu,J.T. [3]
;
Bae,Y. [4]
;
Burrage,L. [5]
;
Turnpenny,P. [6]
;
RománCorona-Rivera,J. [7]
;
Morandi,L. [8]
;
Mora,M. [9]
;
Reutter,H. [10]
;
Vulto-VanSilfhout,A.T. ;
Faivre,L. ;
Haan,E. ;
Gibbs,R.A. ;
Meisler,M.H. ;
Lee,B.H.
作者单位：
Neuromuscular Diseases and Neuroimmunology Unit, Foundation IRCCS Neurological Institute Carlo
[1]
Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX 77030, United States
[2]
Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen 6525, Netherlands
[3]
Centre de Génétique, Centre de Reference Maladies Rares Anomalies du Developpement et Syndromes
[4]
Genetics Service, Division of Pediatrics, Dr. Juan I. Menchaca New Civil Hospital of Guadalajara
[5]
Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109-0618, United States
[6]
Department of Neonatology and Institute of Human Genetics, Children's Hospital, University of Bonn
[7]
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, United
[8]
Clinical Genetics Department, Royal Devon and Exeter Hospital, Exeter EX1 2ED, United Kingdom
[9]
South Australian Clinical Genetics Service, SA Pathology at Women's and Children's Hospital
[10]
发布时间
2013-11-20
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