A gene for autosomal dominant juvenile amyotrophic lateral sclerosis (ALS4 ) localizes to a 500-kb interval on chromosome 9q34 I. P. BlairC. L. BennettP. F. Chance Original article Pages: 1 - 6
The survival motor neuron (SMN) protein: effect of exon loss and mutation on protein localization T. T. LeD. D. CoovertA. H. M. Burghes Original article Pages: 7 - 16
The parental origin of new mutations in neurofibromatosis 2 L. KluweV. MautnerM. MacCollin Original article Pages: 17 - 24
Developmental profile of Sry transcripts in mouse brain A. MayerG. MoslerI. Reisert Original article Pages: 25 - 30
Supporting evidence of a gene for partial epilepsy on 10q V.-F. MautnerM. LindenauL. Kluwe Original article Pages: 31 - 34
Evidence for allelic association of the dopamine β-hydroxylase gene (DBH) with susceptibility to typical migraine R. A. LeaA. DohyL. R. Griffiths Original article Pages: 35 - 40
CLN -encoded proteins do not interact with each other N. A. ZhongD. N. MoroziewiczW. T. Brown Short communication Pages: 41 - 44
Mutation analysis of the hCHK2 gene in primary human malignant gliomas D. N. LouisY. InoD. A. Haber Letter to the editor Pages: 45 - 46
Sequence analysis of the MTCYB gene in Parkinson disease U. von EitzenS. KöselM. B. Graeber Letter to the editor Pages: 47 - 48
Charcot-Marie-Tooth disease and related peripheral neuropathies: novel mutations in the peripheral myelin genes connexin 32 (Cx32 ), peripheral myelin protein 22 (PMP22 ), and peripheral myelin protein zero (MPZ ) A. B. EkiciD. SchweitzerH. Grehl Letter to the editor Pages: 49 - 50