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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

E. Denamur

INSERM U458

Hôpital Robert Debré

and Laboratoire d'Anatomopathologic and EA 3102

Paris

France

[email]@infobiogen.fr

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • INSERM U458, Hôpital Robert Debré, and Laboratoire d'Anatomopathologic and EA 3102, Paris, France. 2000
  • Laboratoire de Biochimie Génétique and Institut National de la Santé et de la Recherche Médicale U458, Hôpital Robert Debré, Paris, France. 1999

References

  1. WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis. Denamur, E., Bocquet, N., Baudouin, V., Da Silva, F., Veitia, R., Peuchmaur, M., Elion, J., Gubler, M.C., Fellous, M., Niaudet, P., Loirat, C. Kidney Int. (2000) [Pubmed]
  2. Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases. Denamur, E., Bocquet, N., Mougenot, B., Da Silva, F., Martinat, L., Loirat, C., Elion, J., Bensman, A., Ronco, P.M. J. Am. Soc. Nephrol. (1999) [Pubmed]
 
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