(Q34392924)
Statements
1 reference
De novo SCN8A mutation identified by whole-exome sequencing in a boy with neonatal epileptic encephalopathy, multiple congenital anomalies, and movement disorders (English)
1 reference
1 reference
Tiit Nikopensius
1 reference
Katrin Ounap
1 reference
Tiia Reimand
1 reference
Ulvi Vaher
1 reference
Margit Nõukas
1 reference
Mart Kals
1 reference
Mari Nelis
1 reference
Inga Talvik
1 reference
Pilvi Ilves
1 reference
Andres Piirsoo
1 reference
Enn Seppet
1 reference
Tiina Talvik
1 reference
18 December 2013
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference