1. The many faces of TUBB4A mutations

   • Katja Lohmann
   • Christine Klein

   Letter to the Editors 21 March 2014 Pages: 81 - 82

2. Reply to: The many faces of TUBB4A mutations

   • Lubov Blumkin
   • Ayelet Halevy
   • Esther Leshinsky-Silver

   Letter to the Editors 23 March 2014 Pages: 83 - 83

3. PIGN mutations cause congenital anomalies, developmental delay, hypotonia, epilepsy, and progressive cerebellar atrophy

   • Chihiro Ohba
   • Nobuhiko Okamoto
   • Hirotomo Saitsu

   Original Article 20 November 2013 Pages: 85 - 92

   

4. Erratum to: PIGN mutations cause congenital anomalies, developmental delay, hypotonia, epilepsy, and progressive cerebellar atrophy

   • Chihiro Ohba
   • Nobuhiko Okamoto
   • Hirotomo Saitsu

   Erratum 19 March 2014 Pages: 93 - 93

5. Partial deletions of the GRN gene are a cause of frontotemporal lobar degeneration

   • Fabienne Clot
   • Anne Rovelet-Lecrux
   • The French clinical and genetic research network on FTLD/FTLD-ALS

   Original Article 28 January 2014 Pages: 95 - 100

   

6. A novel homozygous splicing mutation in PSAP gene causes metachromatic leukodystrophy in two Moroccan brothers

   • Laura Siri
   • Andrea Rossi
   • Mirella Filocamo

   Original Article 31 January 2014 Pages: 101 - 106

   

7. Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene

   • Lubov Blumkin
   • Ayelet Halevy
   • Esther Leshinsky-Silver

   Original Article 14 February 2014 Pages: 107 - 113

   

8. Erratum to: Expansion of the spectrum of TUBB4A-related disorders: A new phenotype associated with a novel mutation in the TUBB4A gene

   • Lubov Blumkin
   • Ayelet Halevy
   • Esther Leshinsky-Silver

   Erratum 21 March 2014 Pages: 115 - 115

9. Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families

   • Gerald Egger
   • Katharina M. Roetzer
   • John B. Vincent

   Original Article 19 March 2014 Pages: 117 - 127

   

10. Assessment of microRNA-related SNP effects in the 3′ untranslated region of the IL22RA2 risk locus in multiple sclerosis

    • Christina M. Lill
    • Marcel Schilling
    • Lars Bertram

    Original Article 18 March 2014 Pages: 129 - 134

    

11. Dysregulated expression of lipid storage and membrane dynamics factors in Tia1 knockout mouse nervous tissue

    • Melanie Vanessa Heck
    • Mekhman Azizov
    • Georg Auburger

    Original Article Open access 23 March 2014 Pages: 135 - 144

    

12. Large APP locus duplication in a sporadic case of cerebral haemorrhage

    • Albert Lladó
    • Oriol Grau-Rivera
    • Anna Antonell

    Short Communication 02 April 2014 Pages: 145 - 149