Publication | Closed Access
CEP290 Mutations Are Frequently Identified in the Oculo-Renal Form of Joubert Syndrome–Related Disorders
156
Citations
27
References
2007
Year
UrologyGenetic DisorderGeneticsInherited Metabolic DiseaseRenal PathologyPathologyCep290 MutationsMolecular GeneticsJoubert Syndrome–related DisordersOculo-renal FormDisease Gene IdentificationMedicineClinical Genetics
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