Deep-phenotyping the less severe spectrum of PIGT deficiency and linking the gene to myoclonic atonic seizures - Bayat, Allan; Pendziwiat, Manuela; Obersztyn, Ewa; Goldenberg, Paula; Zacher, Pia; Driedger, Jan Henje; Syrbe, Steffen; Begtrup, Amber; Borovikov, Artem; Sharkov, Artem; Karasińska, Aneta; Giżewska, Maria; et al. (Frontiers in genetics, 2021)
Gesehen am 21.02.2022