ANOVA, a putative astrocytic RNA-binding protein gene that maps to chromosome 19q13.3 Keisuke UekiShivapriya RamaswamyDavid N. Louis ORIGINAL ARTICLE Pages: 31 - 36
Locus heterogeneity in Friedreich ataxia Markus KostrzewaThomas KlockgetherUlrich Müller ORIGINAL ARTICLE Pages: 43 - 47
Rediscovery of the case described by Alois Alzheimer in 1911: historical, histological and molecular genetic analysis M.B. GraeberS. KöselP. Mehraein ORIGINAL ARTICLE Pages: 73 - 80
SCA2 trinucleotide expansion in German SCA patients Olaf RiessFranco A. LacconeGeorg Auburger ORIGINAL ARTICLE Pages: 59 - 64
A possible role of NAIP gene deletions in sex-related spinal muscular atrophy phenotype variation Giuseppe NovelliSabrina SempriniBruno Dallapiccola SHORT COMMUNICATION Pages: 29 - 30
The genomic organization of human dystrobrevin Hélène M. Sadoulet-PuccioChris A. FeenerLouis M. Kunkel ORIGINAL ARTICLE Pages: 37 - 42
Exon 5 encoded domain is not required for the toxic function of mutant SOD1 but essential for the dismutase activity: identification and characterization of two new SOD1 mutations associated with familial amyotrophic lateral sclerosis James S. ZuHan-Xiang DengTeepu Siddique ORIGINAL ARTICLE Pages: 65 - 71
A model for susceptibility polymorphisms for complex diseases: apolipoprotein E and Alzheimer disease Allen D. Roses REVIEW Pages: 3 - 11
Multiple sclerosis: a polygenic disease involving epistatic interactions, germline rearrangements and environmental effects Marcela V. KarpujLawrence SteinmanJorge R. Oksenberg REVIEW Pages: 21 - 28
Mutations in the δ-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2) David J. DugganDavid ManchesterEric P. Hoffman ORIGINAL ARTICLE Pages: 49 - 58
