Genotype-phenotype correlations in patients with primary ciliary dyskinesia with central complex defects related to RSPH1 , RSPH4A or RSPH9 mutations
B. Prévost, N. Nathan, A. Tamalet, S. Blanchon, G. Montantin, J. F. Papon, E. Kott, L. Bassinet, N. Beydon, N. Collot, B. Copin, F. Dastot, P. Duquesnoy, R. Epaud, I. Honoré, V. Houdouin, S. Tissier, G. Thouvenin, L. Jeanson, B. Vallette, J. de Blic, B. Housset, A. Coste, A. Clément, E. Escudier, S. Amselem, M. Legendre (Paris, Créteil, Toulouse, France)
Source: International Congress 2014 – Molecular pathogenesis of pulmonary inflammatory diseases (COPD, asthma and ILD)
Disease area: Airway diseases, Paediatric lung diseases
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B. Prévost, N. Nathan, A. Tamalet, S. Blanchon, G. Montantin, J. F. Papon, E. Kott, L. Bassinet, N. Beydon, N. Collot, B. Copin, F. Dastot, P. Duquesnoy, R. Epaud, I. Honoré, V. Houdouin, S. Tissier, G. Thouvenin, L. Jeanson, B. Vallette, J. de Blic, B. Housset, A. Coste, A. Clément, E. Escudier, S. Amselem, M. Legendre (Paris, Créteil, Toulouse, France). Genotype-phenotype correlations in patients with primary ciliary dyskinesia with central complex defects related to RSPH1 , RSPH4A or RSPH9 mutations. Eur Respir J 2014; 44: Suppl. 58, 2025
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