Splicing: is there an alternative contribution to Parkinson’s disease? Valentina La CognataVelia D’AgataSebastiano Cavallaro Review article Open access 16 May 2015 Pages: 245 - 263
Variable expression of microglial DAP12 and TREM2 genes in Nasu-Hakola disease Atsushi SasakiAkiyoshi KakitaKei Shioda Original Article 23 May 2015 Pages: 265 - 276
Deletion of Inpp5a causes ataxia and cerebellar degeneration in mice Andy W. YangAndrew J. SachsArne M. Nystuen Original Article 09 June 2015 Pages: 277 - 285
A de novo t(10;19)(q22.3;q13.33) leads to ZMIZ1/PRR12 reciprocal fusion transcripts in a girl with intellectual disability and neuropsychiatric alterations Carlos Córdova-FletesMa. Guadalupe DomínguezVivian Alejandra Neira Original Article 11 July 2015 Pages: 287 - 298
In silico analysis of SIGMAR1 variant (rs4879809) segregating in a consanguineous Pakistani family showing amyotrophic lateral sclerosis without frontotemporal lobar dementia Muhammad Ikram UllahArsalan AhmadMuhammad Jawad Hassan Original Article 24 July 2015 Pages: 299 - 306
Mutations in ARID2 are associated with intellectual disabilities Linshan ShangMegan T. ChoWendy K. Chung Original Article 04 August 2015 Pages: 307 - 314
Novel SIL1 mutations cause cerebellar ataxia and atrophy in a French-Canadian family Anne NoreauRoberta La PianaGuy A. Rouleau Original Article 11 August 2015 Pages: 315 - 318
MRPL44 mutations cause a slowly progressive multisystem disease with childhood-onset hypertrophic cardiomyopathy Felix DistelmaierTobias B. HaackThomas Klopstock Short Communication 24 March 2015 Pages: 319 - 323
Adult-onset glutaric aciduria type I presenting with white matter abnormalities and subependymal nodules T. M. PiersonMani NezhadNancy Sicotte Short Communication 29 August 2015 Pages: 325 - 328