1. A gene for autosomal dominant juvenile amyotrophic lateral sclerosis (ALS4 ) localizes to a 500-kb interval on chromosome 9q34

   • I. P. Blair
   • C. L. Bennett
   • P. F. Chance

   Original article Pages: 1 - 6

2. The survival motor neuron (SMN) protein: effect of exon loss and mutation on protein localization

   • T. T. Le
   • D. D. Coovert
   • A. H. M. Burghes

   Original article Pages: 7 - 16

3. The parental origin of new mutations in neurofibromatosis 2

   • L. Kluwe
   • V. Mautner
   • M. MacCollin

   Original article Pages: 17 - 24

4. Developmental profile of Sry transcripts in mouse brain

   • A. Mayer
   • G. Mosler
   • I. Reisert

   Original article Pages: 25 - 30

5. Supporting evidence of a gene for partial epilepsy on 10q

   • V.-F. Mautner
   • M. Lindenau
   • L. Kluwe

   Original article Pages: 31 - 34

6. Evidence for allelic association of the dopamine β-hydroxylase gene (DBH) with susceptibility to typical migraine

   • R. A. Lea
   • A. Dohy
   • L. R. Griffiths

   Original article Pages: 35 - 40

7. CLN -encoded proteins do not interact with each other

   • N. A. Zhong
   • D. N. Moroziewicz
   • W. T. Brown

   Short communication Pages: 41 - 44

8. Mutation analysis of the hCHK2 gene in primary human malignant gliomas

   • D. N. Louis
   • Y. Ino
   • D. A. Haber

   Letter to the editor Pages: 45 - 46

9. Sequence analysis of the MTCYB gene in Parkinson disease

   • U. von Eitzen
   • S. Kösel
   • M. B. Graeber

   Letter to the editor Pages: 47 - 48

10. 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. Ekici
    • D. Schweitzer
    • H. Grehl

    Letter to the editor Pages: 49 - 50