| No | 記事 | 記事著者 |
|---|
| 1 | Mutations of MLC1(KIAA0027), Encoding a Putative Membrane Protein, Cause Megalencephalic Leukoencephalopathy with Subcortical .. | Peter A.J. Leegwater, Bao Qiang, ... |
| 2 | Cloning if Dimethylglycine Dehydrigenase and a New Human Inborn Error of Metabolism, Dimethylglycine Dehydrogenase Deficiency | Barbara A. Binzak, Ron A. Wevers, ... |
| 3 | Disruption of a Novel Gene(IMMP2L) by a Breakpoint in 7q31 Associated with Tourette Syndrome | Erwin Petek, Christian Windpassinger, ... |
