Rune R. Frants

Functional characterization of compound heterozygosity for GlyRα1 mutations in the startle disease hyperekplexia

D. Kullmann, R. Frants, M. Tijssen, 2002, The European journal of neuroscience.

Genetic Biomarkers for Migraine

R. Frants, B. de Vries, A. M. van den Maagdenberg, 2006, Headache.

The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus

C. Wijmenga, J. Wasmuth, R. Frants, 1993, Human Genetics.

The Phe‐124‐Cys and A‐161T Variants of the Human 5‐HT1B Receptor Gene Are Not Major Determinants of the Clinical Response to Sumatriptan

R. Frants, A. M. van den Maagdenberg, Kaate R. J. Vanmolkot, 2007, Headache.

Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletions.

C. Wijmenga, R. Frants, J. Hewitt, 1994, Genomics.

Hyperekplexia-like syndromes without mutations in the GLRA1 gene

R. Ophoff, J. G. Dijk, M. Tijssen, 1997, Clinical Neurology and Neurosurgery.