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Asma Smahi

Département de Génétique et Unité de Recherches sur les Handicaps Génétiques de l'Enfant INSERM UR-393

Hôpital Necker

149 rue de Sèvres

75743 Paris Cedex 15

France

[email]@necker.fr

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Département de Génétique et Unité de Recherches sur les Handicaps Génétiques de l'Enfant INSERM UR-393, Hôpital Necker, 149 rue de Sèvres, 75743 Paris Cedex 15, France. 2002

References

  1. The NF-kappaB signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes. Smahi, A., Courtois, G., Rabia, S.H., Döffinger, R., Bodemer, C., Munnich, A., Casanova, J.L., Israël, A. Hum. Mol. Genet. (2002) [Pubmed]
 
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