1. Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinoses

   • Sara E. Mole
   • Ruth E. Williams
   • Hans H. Goebel

   Review Article 18 June 2005 Pages: 107 - 126

   

2. The Gem interacting protein (GMIP) gene is associated with major depressive disorder

   • Kazuyuki Tadokoro
   • Ryota Hashimoto
   • Hiroshi Kunugi

   Original Article 06 August 2005 Pages: 127 - 133

   

3. Subcellular localization of spastin: implications for the pathogenesis of hereditary spastic paraplegia

   • Ingrid K. Svenson
   • Mark T. Kloos
   • Douglas A. Marchuk

   Original Article 13 May 2005 Pages: 135 - 141

   

4. Genetic heterogeneity for autosomal recessive pyridoxine-dependent seizures

   • C. L. Bennett
   • H. M. Huynh
   • S. M. Gospe Jr

   Original Article 02 August 2005 Pages: 143 - 149

   

5. Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosis

   • Carol Dobson-Stone
   • Antonio Velayos-Baeza
   • Anthony P. Monaco

   Original Article 26 May 2005 Pages: 151 - 158

   

6. Two missense mutations of EGR2 R359W and GJB1 V136A in a Charcot–Marie–Tooth disease family

   • K. W. Chung
   • I. N. Sunwoo
   • B. O. Choi

   Short Communication 10 June 2005 Pages: 159 - 163

   

7. X-linked creatine transporter deficiency

   • Maria C. Schiaffino
   • Carlo Bellini
   • Eugenio Bonioli

   Short Communication 06 August 2005 Pages: 165 - 168

   

8. A G301R Na⁺/K⁺-ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs

   • Maria Spadaro
   • Simona Ursu
   • Karin Jurkat-Rott

   Erratum 26 August 2005 Pages: 169 - 169