Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia - Inserm - Institut national de la santé et de la recherche médicale Access content directly
Conference Papers Cilia Year : 2012

Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia

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inserm-00752969 , version 1 (16-11-2012)

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  • HAL Id : inserm-00752969 , version 1

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Marie Legendre, Sylvain Blanchon, Bruno Copin, Philippe Duquesnoy, Guy Montantin, et al.. Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia. First International Cilia in Development and Disease Scientific Conference, May 2012, Londres, United Kingdom. pp.P91. ⟨inserm-00752969⟩
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