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概要
論文 | ランダム
- Mutations in the novel protocadherin PCDH15 causes Usher syndrome type 1F
- Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23
- On the time course of perceptual choice: A model based on principles of neural computation
- On the time course of perceptual choice : The leaky competing accumulator model
- A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene