Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3

Author: Tammachote Rachaneekorn   Hommerding Cynthia J.   Sinders Rachel M.   Miller Caroline A.   Czarnecki Peter G.   Leightner Amanda C.   Salisbury Jeffrey L.   Ward Christopher J.   Torres Vicente E.   Gattone Vincent H.   Harris Peter C.  

Publisher: Oxford University Press

E-ISSN: 0964-6906|18|17|3311-3323

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.18, Iss.17, 2009-09, pp. : 3311-3323

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