Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia

1. Marti-Masso, J.F.
2. Ruiz-Martínez, J.
3. Makarov, V.
4. De Munain, A.L.
5. Gorostidi, A.
6. Bergareche, A.
7. Yoon, S.
8. Buxbaum, J.D.
9. Paisán-Ruiz, C.