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Lafora disease in a Malaysian with a rare mutation in the EPM2A gene.
Tee, Sow Kuan; Ong, Tien Lee; Aris, Azman; See, Stephanie Mei Ling; Leong, Huey Yin; Khalid, Mohd Khairul Nizam Mohd; Shanthi, Viswanathan.
Afiliação
  • 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.
Seizure ; 67: 78-81, 2019 Apr.
Article em En | MEDLINE | ID: mdl-30947044
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Lafora / Proteínas Tirosina Fosfatases não Receptoras Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Lafora / Proteínas Tirosina Fosfatases não Receptoras Idioma: En Ano de publicação: 2019 Tipo de documento: Article