A very rare form of autosomal dominant progressive myoclonus epilepsy caused by a novel variant in the PRICKLE1 gene

Bibliographic Details
Title: A very rare form of autosomal dominant progressive myoclonus epilepsy caused by a novel variant in the PRICKLE1 gene
Authors: Algahtani, Hussein, Al-Hakami, Fahad, Al-Shehri, Mohammed, Shirah, Bader, Al-Qahtani, Mohammad H., Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran
Source: In Seizure: European Journal of Epilepsy July 2019 69:133-139
Database: ScienceDirect
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ISSN:10591311
DOI:10.1016/j.seizure.2019.04.016
Published in:Seizure: European Journal of Epilepsy
Language:English