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

Tee SK 1 , Ong TL 2 , Aris A 3 , See SML 4 , Leong HY 5 , Khalid MKNM 6 Show all authors , Shanthi V 7

Affiliations 

  • 1 Department of Neurology, Hospital Kuala Lumpur, Ministry of Health Malaysia, Malaysia. Electronic address: sallytsk83@gmail.com
  • 2 Department of Neurology, Hospital Kuala Lumpur, Ministry of Health Malaysia, Malaysia; Department of Medical, Hospital Sultanah Nur Zahirah, Ministry of Health Malaysia, Malaysia
  • 3 Department of Neurology, Hospital Kuala Lumpur, Ministry of Health Malaysia, Malaysia; Department of Medical, Hospital Melaka, Ministry of Health Malaysia, Malaysia
  • 4 College of Medical and Dental Sciences, University of Birmingham, United Kingdom
  • 5 Department of Genetics, Hospital Kuala Lumpur, Ministry of Health Malaysia, Malaysia
  • 6 Unit of Molecular Diagnostics & Protein, Institute for Medical Research, Ministry of Health Malaysia, Malaysia
  • 7 Department of Neurology, Hospital Kuala Lumpur, Ministry of Health Malaysia, Malaysia
Seizure, 2019 Apr;67:78-81.
PMID: 30947044 DOI: 10.1016/j.seizure.2019.03.012

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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