Neurogenetics presents research that contributes to better understanding of the genetic basis of normal and abnormal function of the nervous system. The journal publishes findings in humans and other organisms that help explain neurological disease mechanisms, and papers from many fields such as biophysics, cell biology, human genetics, neuroanatomy, neurochemistry, neurology, neuropathology, neurosurgery and psychiatry.
Neurogenetics includes Review Articles, Original Articles, Short Communications and Letters to the Editors.
No publication charges except for special services (Open Access, paper offprints, e-offprints, posters etc).
Color art is free of charge for print and online publication.
Whole exome sequencing in Dandy-Walker variant with intellectual disability reveals an activating CIP2A mutation as novel genetic cause
A novel missense variant in the SDR domain of the WWOX gene leads to complete loss of WWOX protein with early-onset epileptic encephalopathy and severe developmental delay
Compound heterozygous mutations in two different domains of ALDH18A1 do not affect the amino acid levels in a patient with hereditary spastic paraplegia
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