Similar target, different effects: late-onset ataxia and spatial learning in prion protein-deficient mouse lines Paolo ValentiAntonio CozzioHans-Peter Lipp Original Article Pages: 173 - 184
Rescue of the Friedreich's ataxia knockout mouse by human YAC transgenesis Mark A. PookSahar Al-MahdawiSusan Chamberlain Original Article Pages: 185 - 193
Linkage and association analysis of chromosome 19q13 in multiple sclerosis Margaret A. Pericak-VanceJacqueline B. RimmlerStephen L. Hauser Original Article Pages: 195 - 201
Mutations in the open reading frame of the β-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease M. Nicolaou Y.-Q. Song E. Rogaeva Original Article Pages: 203 - 206
ACRC codes for a novel nuclear protein with unusual acidic repeat tract and maps to DYT3 (dystonia parkinsonism) critical interval in Xq13.1 Dagmar NolteJuliane RamserUlrich Müller Original Article Pages: 207 - 213
APOE and APOC1 genetic polymorphisms in age-associated memory impairment D. Bartrés-FazI.C. Clemente P. Moral Original Article Pages: 215 - 219
Mapping of a susceptibility gene for multiple sclerosis to the 51 kb interval between G511525 and D6S1666 using a new method of haplotype sharing analysis Maartje BoonIlja M. NolteGerard J. Meerman Original Article Pages: 221 - 230
