Induced pluripotent stem (iPS) cells as in vitro models of human neurogenetic disorders Stormy J. ChamberlainXue-Jun LiMarc Lalande Review Article 13 September 2008 Pages: 227 - 235
Behavioral effects of a deletion in Kcnn2, the gene encoding the SK2 subunit of small-conductance Ca2+-activated K+ channels Marek SzatanikNicolas VibertJean Jaubert Original Article 05 July 2008 Pages: 237 - 248
Nitric oxide synthase genes and their interactions with environmental factors in Parkinson’s disease Dana B. HancockEden R. MartinWilliam K. Scott Original Article 29 July 2008 Pages: 249 - 262
Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease Jung Mi ChoiMyoung Soo WooYun Joong Kim Original Article 15 August 2008 Pages: 263 - 269
The LRRK2 Arg1628Pro variant is a risk factor for Parkinson’s disease in the Chinese population Chin-Song LuYah-Huei Wu-ChouVincenzo Bonifati Original Article Open access 21 August 2008 Pages: 271 - 276
The location of DCX mutations predicts malformation severity in X-linked lissencephaly Pierre-Louis LegerIsabelle SouvilleNadia Bahi-Buisson Original Article 07 August 2008 Pages: 277 - 285
A novel locus for autosomal recessive primary torsion dystonia (DYT17) maps to 20p11.22–q13.12 E. ChoueryJ. KfouryA. Mégarbané Original Article 08 August 2008 Pages: 287 - 293
Identification and characterisation of a large Senataxin (SETX) gene duplication in ataxia with ocular apraxia type 2 (AOA2) Larissa ArningLudger SchölsDagmar Timmann Short Communication 29 July 2008 Pages: 295 - 299
Global distribution of Fatal familial insomnia: founder or recurrent mutations H.-S. LeeL. G. Goldfarb Letter to the Editors 21 June 2008 Pages: 301 - 302
Founder effect and recurrent mutational events in fatal familial insomnia José A. PeñaMiguel A. Alfonso-SánchezMarian M. de Pancorbo Letter to the Editors 21 June 2008 Pages: 303 - 304
