A novel SLC6A8 mutation associated with motor dysfunction in a child exhibiting creatine transporter deficiency

1. Cervera-Acedo, C.
2. Lopez, M.
3. Aguirre-Lamban, J.
4. Santibañez, P.
5. Garcia-Oguiza, A.
6. Poch-Olive, M.L.
7. Dominguez-Garrido, E.