Investigating the genetics of visual processing, function and behaviour in zebrafish Sabine L. RenningerHelia B. SchonthalerRalf Dahm REVIEW ARTICLE 26 January 2011 Pages: 97 - 116
Posterior column ataxia with retinitis pigmentosa in a Japanese family with a novel mutation in FLVCR1 Hiroyuki IshiuraYoko FukudaShoji Tsuji ORIGINAL ARTICLE 26 January 2011 Pages: 117 - 121
New clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS) Jorge L. JuncosJoash T. LazarusStephanie L. Sherman ORIGINAL ARTICLE 29 January 2011 Pages: 123 - 135
A high-penetrance form of late-onset torsion dystonia maps to a novel locus (DYT21) on chromosome 2q14.3-q21.3 Nina NorgrenEmma MattsonMonica Holmberg ORIGINAL ARTICLE 08 February 2011 Pages: 137 - 143
A new missense GDAP1 mutation disturbing targeting to the mitochondrial membrane causes a severe form of AR-CMT2C disease Dagmara KabzińskaAxel NiemannAndrzej Kochański ORIGINAL ARTICLE 02 March 2011 Pages: 145 - 153
C4ORF48, a gene from the Wolf-Hirschhorn syndrome critical region, encodes a putative neuropeptide and is expressed during neocortex and cerebellar development Sabine EndeleClaudia NelkenbrecherAndreas Winterpacht SHORT COMMUNICATION 02 February 2011 Pages: 155 - 163
Identification of a novel CDKL5 exon and pathogenic mutations in patients with severe mental retardation, early-onset seizures and Rett-like features Nils RademacherMelanie HambrockVera M. Kalscheuer LETTER TO THE EDITORS 12 February 2011 Pages: 165 - 167
