Targeted disruption of the Mast syndrome gene SPG21 in mice impairs hind limb function and alters axon branching in cultured cortical neurons Cynthia SoderblomJulia StadlerMichael C. Hanna ORIGINAL ARTICLE 27 July 2010 Pages: 369 - 378
Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafish Laura SouthgateDimitra DafouRichard C. Trembath ORIGINAL ARTICLE Open access 14 April 2010 Pages: 379 - 389
Analysis of NF1 somatic mutations in cutaneous neurofibromas from patients with high tumor burden Laura ThomasLan KluweMeena Upadhyaya ORIGINAL ARTICLE 01 April 2010 Pages: 391 - 400
LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease Carles Vilariño-GüellChristian WiderMatthew J. Farrer ORIGINAL ARTICLE 06 April 2010 Pages: 401 - 408
Analysis of an insertion mutation in a cohort of 94 patients with spinocerebellar ataxia type 31 from Nagano, Japan Haruya SakaiKunihiro YoshidaNaomichi Matsumoto ORIGINAL ARTICLE Open access 28 April 2010 Pages: 409 - 415
Tourette disorder spectrum maps to chromosome 14q31.1 in an Italian kindred Guido J. BreedveldGiovanni FabbriniVincenzo Bonifati ORIGINAL ARTICLE Open access 02 May 2010 Pages: 417 - 423
Myotonic dystrophy type I combined with X-linked dominant Charcot–Marie–Tooth neuropathy Hyun Sook KimKi Wha ChungByung-Ok Choi ORIGINAL ARTICLE 05 May 2010 Pages: 425 - 433
Age at onset in Huntington’s disease: replication study on the associations of ADORA2A, HAP1 and OGG1 Elahe Taherzadeh-FardCarsten SaftLarissa Arning ORIGINAL ARTICLE 30 May 2010 Pages: 435 - 439
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 BoukhrisImed FekiGiovanni Stevanin Original Article 01 July 2010 Pages: 441 - 448
Efficient identification of novel mutations in patients with limb girdle muscular dystrophy Steven E. BoydenMustafa A. SalihPeter B. Kang ORIGINAL ARTICLE Open access 13 July 2010 Pages: 449 - 455
Tremor–ataxia with central hypomyelination (TACH) leukodystrophy maps to chromosome 10q22.3–10q23.31 Geneviève BernardIsabelle ThiffaultBernard Brais ORIGINAL ARTICLE 17 July 2010 Pages: 457 - 464
GJB1/Connexin 32 whole gene deletions in patients with X-linked Charcot–Marie–Tooth disease Claudia Gonzaga-JaureguiFeng ZhangJames R. Lupski SHORT COMMUNICATION 09 June 2010 Pages: 465 - 470
