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Deep-Phenotyping the Less Severe Spectrum of PIGT Deficiency and Linking the Gene to Myoclonic Atonic Seizures
Allan Bayat*, Manuela Pendziwiat, Ewa Obersztyn, Paula Goldenberg, Pia Zacher, Jan Henje Döring, Steffen Syrbe, Amber Begtrup, Artem Borovikov, Artem Sharkov, Aneta Karasińska, Maria Giżewska, Wendy Mitchell, Eva Morava, Rikke S. Møller, Guido Rubboli
*Kontaktforfatter
- Campus Kiel
- Christian-Albrechts-University of Kiel
- Institute of Mother and Child Department of Molecular Genetics
- Massachusetts General Hospital
- The Saxon Epilepsy Center Kleinwachau
- University Hospital Heidelberg
- Research Centre for Medical Genetics
- Pirogov Russian Medical University
- The Nicolas Copernicus State Hospital
- Pomeranian Medical University
- University of Southern California
- Mayo Clinic
- GeneDx, Gaithersburg, Maryland, USA.
- Epilepsihospitalet Filadelfia
- Københavns Universitet
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
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