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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
*Corresponding author for this work
- 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 National Research Medical University (RNRMU).
- The Nicolas Copernicus State Hospital
- Pomeranian Medical University
- University of Southern California
- Mayo Clinic
- GeneDx, Gaithersburg, Maryland, USA.
- Epilepsihospitalet Filadelfia
- University of Copenhagen
Research output: Contribution to journal › Journal article › Research › peer-review
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