| No | 記事 | 記事著者 |
|---|
| 1 | Identification and Expression Analysis of Spastin Gene Mutations in Hereditary Spastic Paraplegia | Ingrid K. Svenson, Allison E. Ashley-Koch, ... |
| 2 | Transaldolase Deficiency: Liver Cirrhosis Associated with a New Inborn Error in the Pentose Phosphate Pathway | Nanda M. Verhoeven, Jojanneke H.J. Huck, ... |
| 3 | MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin | R. Trappe, F. Laccone, J. Cobilanschi, ... |
