DOI: 10.1055/s-00000071

Seminars in Neurology

LinksClose Window

References

Lund C, Brodtkorb E, Øye AM, Røsby O, Selmer KK.
CHD2 mutations in Lennox-Gastaut syndrome.

Epilepsy Behav 2014;
33: 18-21

Download Bibliographical Data

Access:
Access:

We do not assume any responsibility for the contents of the web pages of other providers.