作者：
Hopkin, Robert J. [1]
;
Cabrera, Gustavo [2]
;
Charrow, Joel [3]
;
Lemay, Roberta [4]
;
Martins, Ana Maria [5]
;
Mauer, Michael [6]
;
Ortiz, Alberto [7]
;
Patel, Manesh R. [8]
;
Sims, Katherine [9]
;
Waldek, Stephen [10]
;
Warnock, David G. [11]
;
Wilcox, William R. [12]
作者单位：
UAM, IIS Fdn Jimenez Diaz, Sch Med, Unidad Dialisis,IRSIN,REDINREN, Madrid, Spain
[1]
Emory Univ, Sch Med, Dept Human Genet, Div Med Genet, Atlanta, GA USA
[2]
Ann & Robert H Lurie Childrens Hosp Chicago, Div Genet Birth Defects & Metab, Chicago, IL 60611 USA
[3]
Sanofi Genzyme, Rare Dis, Strateg Epidemiol & Biostat, Cambridge, MA USA
[4]
Univ Fed Sao Paulo, Reference Ctr Inborn Errors Metab, Sao Paulo, Brazil
[5]
Univ Minnesota, Dept Pediat, Minneapolis, MN 55455 USA
[6]
Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
[7]
Univ Sunderland, Sunderland SR2 7EE, Durham, England
[8]
Ctr Cardiovasc Bolivar, Buenos Aires, DF, Argentina
[9]
Duke Univ, Sch Med, Div Cardiovasc Med, Durham, NC 27706 USA
[10]
Univ Alabama Birmingham, Div Nephrol, Birmingham, AL USA
[11]
Cincinnati Childrens Hosp Med Ctr, 3333 Burnet Ave, Cincinnati, OH 45229 USA
[12]
发布时间
2017-09-26
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