Seneste publikationer Vis alle (3) »

1. E-pub ahead of print

   Familial analysis reveals rare risk variants for migraine in regulatory regions

   Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

2. Udgivet

   Compound heterozygous mutations in two different domains of ALDH18A1 do not affect the amino acid levels in a patient with hereditary spastic paraplegia

   Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

3. Udgivet

   Chromosomal rearrangements in Tourette syndrome: implications for identification of candidate susceptibility genes and review of the literature

   Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review