| No | 記事 | 記事著者 |
|---|
| 1 | Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F | Zubair M. Ahmed, Saima Riazuddin, ... |
| 2 | Disorders of Peroxisome Biogenesis Due to Mutations in PEX1: Phenotypes and PEX1 Protein Levels | Claudia Walter, Jeannette Gootjes, ... |
| 3 | Gene Mutations in the Succinate Dehydrogenase Subunit SDHB Cause Susceptibility to Familial Pheocheromocytoma and to Familial .. | Dewi Astuti, Farida Latif, Ashraf Dallol, ... |
