| No | 記事 | 記事著者 |
|---|
| 1 | Mutations in FOXC2(MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis .. | Jianming Fang, Susan L. Dagenais, ... |
| 2 | Mitochondrial Encephalomyopathy and Complex 3 Deficiency Associated with a Stop-Codon Mutation in the Cytochrome b Gene | J. Andrew Keightley, Roberto Anitori, ... |
| 3 | Molecular Characterization of 3-Phosphoglycerate Dehydrogenase Deficiency -- a Neurometabolic Disorder Associated ... | Leo W.J. Klomp, Tom J. de Koning, ... |
