作者：
Meyer,E. [1]
;
Kurian,M.A. [2]
;
Morgan,N.V. [3]
;
McNeill,A. [4]
;
Pasha,S. [5]
;
Tee,L. ;
Younis,R. ;
Norman,A. ;
vanderKnaap,M.S. ;
Wassmer,E. ;
Trembath,R.C. ;
Brueton,L. ;
Maher,E.R.
作者单位：
Department of Paediatric Neurology, Birmingham Children's Hospital, Birmingham, United Kingdom
[1]
Department of Medical and Molecular Genetics, Institute of Biomedical Research, Centre for Rare
[2]
Department of Child Neurology, VU University Medical Center, Amsterdam, Netherlands
[3]
West Midlands Region Genetics Service, Birmingham Women's Hospital NHS Foundation Trust, Birmingham
[4]
Department of Medical and Molecular Genetics, King's College London, School of Medicine, Guy's
[5]
发布时间
2013-11-20
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