1. Targeted disruption of the Mast syndrome gene SPG21 in mice impairs hind limb function and alters axon branching in cultured cortical neurons

   • Cynthia Soderblom
   • Julia Stadler
   • Michael C. Hanna

   ORIGINAL ARTICLE 27 July 2010 Pages: 369 - 378

   

2. Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafish

   • Laura Southgate
   • Dimitra Dafou
   • Richard C. Trembath

   ORIGINAL ARTICLE Open access 14 April 2010 Pages: 379 - 389

   

3. Analysis of NF1 somatic mutations in cutaneous neurofibromas from patients with high tumor burden

   • Laura Thomas
   • Lan Kluwe
   • Meena Upadhyaya

   ORIGINAL ARTICLE 01 April 2010 Pages: 391 - 400

   

4. LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease

   • Carles Vilariño-Güell
   • Christian Wider
   • Matthew J. Farrer

   ORIGINAL ARTICLE 06 April 2010 Pages: 401 - 408

   

5. Analysis of an insertion mutation in a cohort of 94 patients with spinocerebellar ataxia type 31 from Nagano, Japan

   • Haruya Sakai
   • Kunihiro Yoshida
   • Naomichi Matsumoto

   ORIGINAL ARTICLE Open access 28 April 2010 Pages: 409 - 415

   

6. Tourette disorder spectrum maps to chromosome 14q31.1 in an Italian kindred

   • Guido J. Breedveld
   • Giovanni Fabbrini
   • Vincenzo Bonifati

   ORIGINAL ARTICLE Open access 02 May 2010 Pages: 417 - 423

   

7. Myotonic dystrophy type I combined with X-linked dominant Charcot–Marie–Tooth neuropathy

   • Hyun Sook Kim
   • Ki Wha Chung
   • Byung-Ok Choi

   ORIGINAL ARTICLE 05 May 2010 Pages: 425 - 433

   

8. Age at onset in Huntington’s disease: replication study on the associations of ADORA2A, HAP1 and OGG1

   • Elahe Taherzadeh-Fard
   • Carsten Saft
   • Larissa Arning

   ORIGINAL ARTICLE 30 May 2010 Pages: 435 - 439

9. A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum

   • Amir Boukhris
   • Imed Feki
   • Giovanni Stevanin

   Original Article 01 July 2010 Pages: 441 - 448

   

10. Efficient identification of novel mutations in patients with limb girdle muscular dystrophy

    • Steven E. Boyden
    • Mustafa A. Salih
    • Peter B. Kang

    ORIGINAL ARTICLE Open access 13 July 2010 Pages: 449 - 455

    

11. Tremor–ataxia with central hypomyelination (TACH) leukodystrophy maps to chromosome 10q22.3–10q23.31

    • Geneviève Bernard
    • Isabelle Thiffault
    • Bernard Brais

    ORIGINAL ARTICLE 17 July 2010 Pages: 457 - 464

    

12. GJB1/Connexin 32 whole gene deletions in patients with X-linked Charcot–Marie–Tooth disease

    • Claudia Gonzaga-Jauregui
    • Feng Zhang
    • James R. Lupski

    SHORT COMMUNICATION 09 June 2010 Pages: 465 - 470

    

13. Acknowledgement to Referees 2009/2010

    ACKNOWLEDGEMENT TO REFEREES 21 September 2010 Pages: 471 - 471