| No | 記事 | 記事著者 |
|---|
| 1 | Autosomal Dominant Craniometaphyseal Dysplasia Is Caused by Mutations in the Transmembrabe Protein ANK | Ernst Reichenberger, Valdenize Tiziani, ... |
| 2 | De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy | Lieve Claes, Jurgen Del-Favero, ... |
| 3 | Large-Scale Deletion and Point Mutations of the Nuclear NDUFV1 and NDUFS1 Genes in Mitochondrial Complex 1 Deficiency | Paule Benit, Dominique Chreiten, ... |
