Neurogenetics
A novel locus for restless legs syndrome maps to chromosome 19p in an Irish pedigree
Axonal transport deficit in a KIF5A –/– mouse model
Forkhead family transcription factor FoxO and neural differentiation
Frequency of SMARCB1 mutations in familial and sporadic schwannomatosis
JPH3 repeat expansions cause a progressive akinetic-rigid syndrome with severe dementia and putaminal rim in a five-generation African-American family
Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores
Regulation of estrogen receptor alpha gene expression in the mouse prefrontal cortex during early postnatal development
Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients
Systems genetic analysis of the effects of iron deficiency in mouse brain