Table of contents

Original articles

• Association between a common mitochondrial DNA D-loop polycytosine variant and alteration of mitochondrial copy number in human peripheral blood cells (12 September, 2010)

  C-W Liou, T-K Lin, J-B Chen, M-M Tiao, S-W Weng, S-D Chen, Y-C Chuang, J-H Chuang, P-W Wang
• Guanosine diphosphate-mannose:GlcNAc₂-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutations

  (2 August, 2010)

  T Dupré, S Vuillaumier-Barrot, I Chantret, H S Yayé, C Le Bizec, A Afenjar, C Altuzarra, C Barnérias, L Burglen, P de Lonlay, F Feillet, S Napuri, N Seta, S E H Moore
• Wide spectrum of desmosomal mutations in Danish patients with arrhythmogenic right ventricular cardiomyopathy (23 September, 2010)

  A H Christensen, M Benn, H Bundgaard, A Tybjærg-Hansen, S Haunso, J H Svendsen
• FSH dystrophy and a subtelomeric 4q haplotype: a new assay and associations with disease (15 August, 2010)

  K Tsumagari, D Chen, J R Hackman, A D Bossler, M Ehrlich
• ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism

  (3 August, 2010)

  C Bellanné-Chantelot, C Saint-Martin, M-J Ribeiro, C Vaury, V Verkarre, J-B Arnoux, V Valayannopoulos, S Gobrecht, C Sempoux, J Rahier, J-C Fournet, F Jaubert, Y Aigrain, C Nihoul-Fékété, P de Lonlay
• Epigenotype–phenotype correlations in Silver–Russell syndrome (3 August, 2010)

  E L Wakeling, S Abu Amero, M Alders, J Bliek, E Forsythe, S Kumar, D H Lim, F MacDonald, D J Mackay, E R Maher, G E Moore, R L Poole, S M Price, T Tangeraas, C L S Turner, M M Van Haelst, C Willoughby, I K Temple, J M Cobben