Ccdc66 null mutation causes retinal degeneration and dysfunction

Author: Gerding Wanda M.   Schreiber Sabrina   Schulte-Middelmann Tobias   de Castro Marques Andreia   Atorf Jenny   Akkad Denis A.   Dekomien Gabriele   Kremers Jan   Dermietzel Rolf   Gal Andreas   Rülicke Thomas   Ibrahim Saleh   Epplen Jörg T.   Petrasch-Parwez Elisabeth  

Publisher: Oxford University Press

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.20, Iss.18, 2011-09, pp. : 3620-3631

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Abstract