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                                       Details for article 10 of 20 found articles
 
 
  Loss-of-Function Mutations in RSPH1 Cause Primary Ciliary Dyskinesia with Central-Complex and Radial-Spoke Defects
 
 
Title: Loss-of-Function Mutations in RSPH1 Cause Primary Ciliary Dyskinesia with Central-Complex and Radial-Spoke Defects
Author: Kott, Esther
Legendre, Marie
Copin, Bruno
Papon, Jean-François
Dastot-Le Moal, Florence
Montantin, Guy
Duquesnoy, Philippe
Piterboth, William
Amram, Daniel
Bassinet, Laurence
Beucher, Julie
Beydon, Nicole
Deneuville, Eric
Houdouin, Véronique
Journel, Hubert
Just, Jocelyne
Nathan, Nadia
Tamalet, Aline
Collot, Nathalie
Jeanson, Ludovic
Le Gouez, Morgane
Vallette, Benoit
Vojtek, Anne-Marie
Epaud, Ralph
Coste, André
Clement, Annick
Housset, Bruno
Louis, Bruno
Escudier, Estelle
Amselem, Serge
Appeared in: The American journal of human genetics
Paging: Volume 93 (2013) nr. 3 pages 10 p.
Year: 2013
Contents:
Publisher: The American Society of Human Genetics
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 10 of 20 found articles
 
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