1. Investigating the genetics of visual processing, function and behaviour in zebrafish

   • Sabine L. Renninger
   • Helia B. Schonthaler
   • Ralf Dahm

   REVIEW ARTICLE 26 January 2011 Pages: 97 - 116

   

2. Posterior column ataxia with retinitis pigmentosa in a Japanese family with a novel mutation in FLVCR1

   • Hiroyuki Ishiura
   • Yoko Fukuda
   • Shoji Tsuji

   ORIGINAL ARTICLE 26 January 2011 Pages: 117 - 121

   

3. New clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS)

   • Jorge L. Juncos
   • Joash T. Lazarus
   • Stephanie L. Sherman

   ORIGINAL ARTICLE 29 January 2011 Pages: 123 - 135

4. A high-penetrance form of late-onset torsion dystonia maps to a novel locus (DYT21) on chromosome 2q14.3-q21.3

   • Nina Norgren
   • Emma Mattson
   • Monica Holmberg

   ORIGINAL ARTICLE 08 February 2011 Pages: 137 - 143

   

5. A new missense GDAP1 mutation disturbing targeting to the mitochondrial membrane causes a severe form of AR-CMT2C disease

   • Dagmara Kabzińska
   • Axel Niemann
   • Andrzej Kochański

   ORIGINAL ARTICLE 02 March 2011 Pages: 145 - 153

   

6. C4ORF48, a gene from the Wolf-Hirschhorn syndrome critical region, encodes a putative neuropeptide and is expressed during neocortex and cerebellar development

   • Sabine Endele
   • Claudia Nelkenbrecher
   • Andreas Winterpacht

   SHORT COMMUNICATION 02 February 2011 Pages: 155 - 163

   

7. Identification of a novel CDKL5 exon and pathogenic mutations in patients with severe mental retardation, early-onset seizures and Rett-like features

   • Nils Rademacher
   • Melanie Hambrock
   • Vera M. Kalscheuer

   LETTER TO THE EDITORS 12 February 2011 Pages: 165 - 167