Publication | Open Access
CC2D2A Is Mutated in Joubert Syndrome and Interacts with the Ciliopathy-Associated Basal Body Protein CEP290
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Citations
38
References
2008
Year
Molecular NeuroscienceJoubert SyndromeMedicineGeneticsGenetic DisorderPathologyDisease Gene IdentificationNeuromuscular PathologyCc2d2a Is MutatedNeurogenetics
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