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Archives de pédiatrie
Volume 20, n° 4
pages 429-430 (avril 2013)
Doi : 10.1016/j.arcped.2013.01.046
Phénotype clinique reconnaissable des neurodegeneration with brain iron accumulation (NBIA) liées aux mutations du gène C19ORF12
 

A. Afenjar a, b, c, , T. Billette De Villemeur a, b, B. Chabrol d, D. Gras e, A. Legall c, F. Mochel f, F. Sedel g, D. Rodriguez a, b, L. Burglen a, c
a Centre de référence malformations et maladies congénitales du cervelet, hôpital Trousseau, Paris, France 
b Neuropédiatrie, hôpital Trousseau, Paris, France 
c Génétique, hôpital Trousseau et Inserm U676, Paris, France 
d Centre de référence maladies héréditaires du métabolisme, hôpital La Timone, Marseille, France 
e Neuropédiatrie, hôpital Robert-Debré, Paris, France 
f Génétique, hôpital Pitié-Salpêtrière, Paris, France 
g Neurologie, hôpital Pitié-Salpêtrière, Paris, France 

Auteur correspondant.


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