1. Developing the field of neurogenetics

   • Ulrich Müller
   • Georg Auburger
   • Louis J. Ptacek

   Editorial 21 November 2017 Pages: 183 - 184

2. X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1

   • Noriko Miyake
   • Nicole I. Wolf
   • Adeline Vanderver

   Original Article Open access 26 August 2017 Pages: 185 - 194

   

3. Molecular diversity of combined and complex dystonia: insights from diagnostic exome sequencing

   • Michael Zech
   • Robert Jech
   • Juliane Winkelmann

   Original Article 28 August 2017 Pages: 195 - 205

   

4. Molecular genetic and clinical characterization of myotonic dystrophy type 1 patients carrying variant repeats within DMPK expansions

   • Jovan Pešović
   • S. Perić
   • Dušanka Savić-Pavićević

   Original Article 23 September 2017 Pages: 207 - 218

   

5. Coexistence of CLCN1 and SCN4A mutations in one family suffering from myotonia

   • Lorenzo Maggi
   • Sabrina Ravaglia
   • Massimiliano Filosto

   Original Article 09 October 2017 Pages: 219 - 225

   

6. Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits

   • Ruth I. C. Glasgow
   • Kyle Thompson
   • Robert W. Taylor

   Original Article Open access 26 October 2017 Pages: 227 - 235

   

7. GNE missense mutation in recessive familial amyotrophic lateral sclerosis

   • Çiğdem Köroğlu
   • Rezzak Yılmaz
   • Özden Şener

   Original Article 31 October 2017 Pages: 237 - 243

   

8. A newly distal hereditary motor neuropathy caused by a rare AIFM1 mutation

   • Paula Sancho
   • Ana Sánchez-Monteagudo
   • Vincenzo Lupo

   Short Communication 03 October 2017 Pages: 245 - 250

   

9. Acknowledgement to Referees 2016/2017

   Acknowledgement to Referee 11 September 2017 Pages: 251 - 251