作者：
Nambot, S. [1]
;
Gavrilov, D. [2]
;
Thevenon, J. [3]
;
Bruel, A. L. [4]
;
Bainbridge, M. [5]
;
Rio, M. [6]
;
Goizet, C. [7]
;
Rotig, A. [8]
;
Jaeken, J. [9]
;
Niu, N. [10]
;
Xia, F. [11]
;
Vital, A. [12]
;
Houcinat, N. ;
Mochel, F. ;
Kuentz, P. ;
Lehalle, D. ;
Duffourd, Y. ;
Riviere, J. B. ;
Thauvin-Robinet, C. ;
Beaudet, A. L. ;
Faivre, L.
作者单位：
CHU Dijion, Lab Genet Mol, Plateau Tech Biol, Dijon, France
[1]
Hop Necker Enfants Malad, Inst Rech Necker Enfants Malad, Lab Genet Mol, Paris, France
[2]
CHU Bordeaux GH Pellegrin, Serv Pathol, Pole Biol & Pathol, Bordeaux, France
[3]
Hop Necker Enfants Malad, Serv Genet Med, Paris, France
[4]
CHU Bordeaux GH Pellegrin, Serv Genet Med, Bordeaux, France
[5]
Univ Hosp Gasthuisberg, Ctr Metab Dis, Leuven, Belgium
[6]
Mayo Clin, Dept Lab Med & Pathol, Biochem Genet Lab, Coll Med, Rochester, MN USA
[7]
CHU La Pitie Salpetriere Charles Foix, Serv Genet Med, Paris, France
[8]
Baylor Coll Med, Human Genome Sequencing Ctr, Houston, TX 77030 USA
[9]
CHU Dijion, Hop Enfants, Ctr Genet, Dijon, France
[10]
Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[11]
CHU Dijon, Federat Hosp Univ Med Translat & Anomalies Dev FH, Dijon, France
[12]
发布时间
2018-01-30
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