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2. Contributors

13. Expanding the spectrum of CEP55 ‐associated disease to viable phenotypes

14. Mutations in PLS1 , encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss

20. Human Bacterial Artificial Chromosome (BAC) Transgenesis Fully Rescues Noradrenergic Function in Dopamine β-Hydroxylase Knockout Mice

23. Regulatory Polymorphisms in Human DBH Affect Peripheral Gene Expression and Sympathetic Activity

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