DOI: 10.1055/s-00000071

Seminars in Neurology

LinksSchließen

Referenz

Syrbe S, Hedrich UB, Riesch E , et al.
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy.

Nat Genet 2015;
4 (4) 393-399

Bibliographische Angaben herunterladen

Suchen in: