Lafora disease in a Malaysian with a rare mutation in the EPM2A gene.

Autor: Tee SK; Department of Neurology, Hospital Kuala Lumpur, Ministry of Health Malaysia, Malaysia. Electronic address: sallytsk83@gmail.com., Ong TL; Department of Neurology, Hospital Kuala Lumpur, Ministry of Health Malaysia, Malaysia; Department of Medical, Hospital Sultanah Nur Zahirah, Ministry of Health Malaysia, Malaysia., Aris A; Department of Neurology, Hospital Kuala Lumpur, Ministry of Health Malaysia, Malaysia; Department of Medical, Hospital Melaka, Ministry of Health Malaysia, Malaysia., See SML; College of Medical and Dental Sciences, University of Birmingham, United Kingdom., Leong HY; Department of Genetics, Hospital Kuala Lumpur, Ministry of Health Malaysia, Malaysia., Khalid MKNM; Unit of Molecular Diagnostics & Protein, Institute for Medical Research, Ministry of Health Malaysia, Malaysia., Shanthi V; Department of Neurology, Hospital Kuala Lumpur, Ministry of Health Malaysia, Malaysia.
Jazyk: angličtina
Zdroj: Seizure [Seizure] 2019 Apr; Vol. 67, pp. 78-81. Date of Electronic Publication: 2019 Mar 25.
DOI: 10.1016/j.seizure.2019.03.012
Databáze: MEDLINE
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