作者：
Burgard, Peter [1]
;
Ullrich, Kurt [2]
;
Ballhausen, Diana [3]
;
Hennermann, Julia B. [4]
;
Hollak, Carla E. M. [5]
;
Langeveld, Mirjam [6]
;
Karall, Daniela [7]
;
Konstantopoulou, Vassiliki [8]
;
Maier, Esther M. [9]
;
Lang, Frauke [10]
;
Lachmann, Robin [11]
;
Murphy, Elaine ;
Garbade, Sven ;
Hoffmann, Georg F. ;
Koelker, Stefan ;
Lindner, Martin ;
Zschocke, Johannes
作者单位：
Johannes Gutenberg Univ Mainz, Ctr Paediat & Adolescent Med, Mainz, Germany
[1]
CHUV BT 02 252, Serv Med Genet, Ctr Malad Mol, Lausanne, Switzerland
[2]
Med Univ Vienna, Dept Pediat & Adolescent Med, Vienna, Austria
[3]
Med Univ Innsbruck, Pediat Clin, Inherited Metab Disorders, Innsbruck, Austria
[4]
Heidelberg Univ Hosp, Div Neuropaediat & Metab Med, Ctr Paediat & Adolescent Med, D-69120
[5]
Univ Childrens Hosp Frankfurt, Frankfurt, Germany
[6]
Natl Hosp Neurol & Neurosurg, Charles Dent Metab Unit, London, England
[7]
Acad Med Ctr, Div Clin Endocrinol & Metab, Amsterdam, Netherlands
[8]
Med Univ Innsbruck, Div Human Genet, Innsbruck, Austria
[9]
Univ Med Ctr Hamburg Eppendorf, Int Ctr Lysosomal Disorders, Univ Ctr Rare Dis, Hamburg, Germany
[10]
Univ Munich, Dr von Hauner Childrens Hosp, Munich, Germany
[11]
发布时间
2017-10-18
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