作者：
Borgwardt, Line [1]
;
Guffon, Nathalie [2]
;
Amraoui, Yasmina [3]
;
Dali, Christine I. [4]
;
De Meirleir, Linda [5]
;
Gil-Campos, Mercedes [6]
;
Heron, Benedicte [7]
;
Geraci, Silvia [8]
;
Ardigo, Diego [9]
;
Cattaneo, Federica [10]
;
Fogh, Jens [11]
;
Van den Hout, J. M. Hannerieke [12]
;
Beck, Michael [13]
;
Jones, Simon A. ;
Tylki-Szymanska, Anna ;
Haugsted, Ulla ;
Lund, Allan M.
作者单位：
Hop Femme Mere Enfant, Ctr Reference Malad Hereditaires Metab, Lyon, France
[1]
Univ Med Ctr, Inst Human Genet, Mainz, Germany
[2]
Univ Med Ctr Mainz, Ctr Pediat & Adolescent Med, Villa Metab, Mainz, Germany
[3]
Ctr Inherited Metab Dis, Dept Paediat & Adolescent Med, Copenhagen, Denmark
[4]
Copenhagen Univ Hosp, Rigshosp, Dept Occupat Therapy & Physiotherapy, Copenhagen, Denmark
[5]
UPMC Univ 06, Sorbonne Univ, Reference Ctr Lysosomal Dis, Trousseau Hosp,APHP,Dept Pediat Nerol
[6]
Erasmus MC Univ, Med Ctr, Sophia Childrens Hosp, Ctr Lysosomal & Metab Dis,Dept Pediat, Rotterdam
[7]
Chiesi Farmaceutici SpA, Parma, Italy
[8]
Childrens Mem Hlth Inst, Dept Paediat Nutr & Metab Dis, Warsaw, Poland
[9]
Univ Ziekenhuis, Paediat Neurol & Metab, Brussels, Belgium
[10]
Univ Cordoba, CIBERObn, Unidad Metab & Invest Pediat, Hosp Univ Reina Sofia IMIBIC, Cordoba, Spain
[11]
Zymenex AS, Hillerod, Denmark
[12]
Cent Manchester Univ Hosp NHS Fdn Trust, Manchester Ctr Genom Med, Manchester, Lancs, England
[13]
发布时间
2019-06-06
换一批
