Gorden et al., 2008 - CC2D2A Is Mutated in Joubert Syndrome and Interacts with the Ciliopathy-Associated Basal Body Protein CEP290. American journal of human genetics   83(5):559-571 Full text @ Am. J. Hum. Genet.
4 Genes / Markers
Marker Type Symbol Name
Gene cc2d2a coiled-coil and C2 domain containing 2A
Gene cep290 centrosomal protein 290
Gene cep76 centrosomal protein 76
Gene odc1 ornithine decarboxylase 1
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