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Association of common genetic variants with vitamin D status in Malaysian children with epilepsy.
Kong, Ann Nie; Fong, Choong Yi; Ng, Ching Ching; Mohamed, Ahmad Rithauddin; Khoo, Teik Beng; Ng, Rui Lun; Jalaludin, Muhammad Yazid; Nadarajaw, Thiyagar.
Afiliação
  • Kong AN; Division of Paediatric Neurology, Department of Paediatrics, Faculty of Medicine, University Malaya, Kuala Lumpur, Malaysia.
  • Fong CY; Division of Paediatric Neurology, Department of Paediatrics, Faculty of Medicine, University Malaya, Kuala Lumpur, Malaysia. Electronic address: cyfong@ummc.edu.my.
  • Ng CC; Genetics and Molecular Biology, Institute of Biological Sciences, Faculty of Science, University of Malaya, Kuala Lumpur, Malaysia.
  • Mohamed AR; Paediatric Neurology Unit, Women and Children's Hospital, Kuala Lumpur, Malaysia.
  • Khoo TB; Paediatric Neurology Unit, Women and Children's Hospital, Kuala Lumpur, Malaysia.
  • Ng RL; Division of Paediatric Neurology, Department of Paediatrics, Faculty of Medicine, University Malaya, Kuala Lumpur, Malaysia; Paediatric Department, Hospital Sultanah Bahiyah, Alor Setar, Kedah, Malaysia.
  • Jalaludin MY; Division of Pediatric Endocrinology, Department of Pediatrics, Faculty of Medicine, University Malaya, Kuala Lumpur, Malaysia.
  • Nadarajaw T; Paediatric Department, Hospital Sultanah Bahiyah, Alor Setar, Kedah, Malaysia.
Seizure ; 79: 103-111, 2020 Jul.
Article em En | MEDLINE | ID: mdl-32464532
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vitamina D / Deficiência de Vitamina D / Epilepsia Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vitamina D / Deficiência de Vitamina D / Epilepsia Idioma: En Ano de publicação: 2020 Tipo de documento: Article