All Relations between ds and scn1a
| Publication | Sentence | Publish Date | Extraction Date | Species |
|---|---|---|---|---|
| Rima Nabbout, Christel Depienne, Mathilde Chipaux, Benoit Girard, Isabelle Souville, Oriane Trouillard, Olivier Dulac, Jamel Chelly, Alexandra Afenjar, Delphine Héron, Eric Leguern, Cherif Beldjord, Thierry Bienvenu, Nadia Bahi-Buisso. CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancy. Epilepsy research. vol 87. issue 1. 2010-01-05. PMID:19734009. | severe myoclonic epilepsy of infancy (smei) or dravet syndrome (ds) is a distinctive epilepsy syndrome often associated with de novo mutations in the scn1a gene. | 2010-01-05 | 2023-08-12 | Not clear |