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2. Opportunities and Challenges for Molecular Understanding of Ciliopathies–The 100,000 Genomes Project

3. Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

5. A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

6. Editorial comment

7. Association between p47phox pseudogenes and inflammatory bowel disease

8. Erratum

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