作者：
Harlalka, Gaurav V. [1]
;
McEntagart, Meriel E. [2]
;
Gupta, Neerja [3]
;
Skrzypiec, Anna E. [4]
;
Mucha, Mariusz W. [5]
;
Chioza, Barry A. [6]
;
Simpson, Michael A. [7]
;
Sreekantan-Nair, Ajith [8]
;
Pereira, Anthony ;
Guenther, Sven ;
Jahic, Amir ;
Modarres, Hamid ;
Moore-Barton, Heather ;
Trembath, Richard C. ;
Kabra, Madhulika ;
Baple, Emma L. ;
Thakur, Seema ;
Patton, Michael A. ;
Beetz, Christian ;
Pawlak, Robert ;
Crosby, Andrew H.
作者单位：
All India Inst Med Sci, Div Genet, Dept Pediat, Old OT Block, New Delhi, India
[1]
Univ Exeter, Royal Devon & Exeter NHS Fdn Trust, RILD Wellcome Wolfson Ctr, Sch Med, Barrack Rd
[2]
St Georges Univ London, Med Genet Unit, Floor 0,Jenner Wing,Cranmer Terrace, London, England
[3]
Fortis La Femme, Dept Genet & Fetal Med, S-549, New Delhi, India
[4]
Univ Exeter, Sch Med, Lab Neuronal Plast & Behav, Exeter, Devon, England
[5]
St George Hosp, Dept Neurol, Atkinson Morley Wing, London, England
[6]
Jena Univ Hosp, Dept Clin Chem & Lab Med, Jena, Germany
[7]
Kings Coll London, Guys Hosp, Sch Med, Div Genet & Mol Med, London, England
[8]
发布时间
2017-04-06
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