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White Matter Disorders - Classification White Matter Disorders - Classification
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  3. White Matter Disorders - Classification
  4. Sequence primers for new disorders

Sequence primers for new disorders

  • About the Center
    • A parents' story
    • Address and contact
  • About the foundation
  • White matter disorders - Introduction
    • Glossary
    • Diagnosis
      • Magnetic Resonance background
    • Patient care
    • Inheritance
  • White Matter Disorders - Classification
    • Acquired white matter disorders
    • Hereditary white matter disorders - Classified
      • Metachromatic leukodystrophy
      • Krabbe disease
    • Hereditary white matter disorders - Unclassified
    • Sequence primers for new disorders
    • 'New' white matter disorders
      • Vanishing white matter disease
      • Leukoencephalopathy with brain stem and spinal cord involvement and elevated lactate
      • Megalencephalic leukoencephalopathy with subcortical cysts
      • 4H syndrome
      • Hypomyelination with atrophy of the basal ganglia and cerebellum
      • Defects in polyol metabolism
  • Supplementary data
    • Multiple Sclerosis Journal, Pronk et al. 2008
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Sequence primers

The primers for sequencing exons and surrounding intronic regions for the genes involved in Vanishing White Matter disease (EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5), Megalencephalic Leukoencephalopathy with Subcortical Cysts (MLC1), and Leukoencephalopathy with Brain Stem and Spinal Cord Involvement with Elevated Lactate (DARS2) are given in the excel files indicated below.

Location VUmc / De Boelelaan

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