Table of contents

Original articles

• Polymorphisms in C2, CFB and C3 are associated with progression to advanced age related macular degeneration associated with visual loss

  (17 November, 2008)

  P J Francis, S C Hamon, J Ott, R G Weleber, M L Klein
• Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genes (2 February, 2009)

  S M Ware, N El-Hassan, S G Kahler, Q Zhang, Y-W, E Miller, B Wong, R L Spicer, W J Craigen, B A Kozel, D K Grange, L-J Wong
• Replication of restless legs syndrome loci in three European populations (10 March, 2009)

  D Kemlink, O Polo, B Frauscher, V Gschliesser, B Högl, W Poewe, P Vodicka, J Vavrova, K Sonka, S Nevsimalova, B Schormair, P Lichtner, K Silander, L Peltonen, C Gieger, H E Wichmann, A Zimprich, D Roeske, B Müller-Myhsok, T Meitinger, J Winkelmann
• Evaluation of a surveillance programme for women with a family history of breast cancer (10 March, 2009)

  M M Reis, M Tavakoli, J Dewar, D Goudie, A Cook, L McLeish, D Young, J Kenyon, M Steel
• Premature death in adults with 22q11.2 deletion syndrome (25 February, 2009)

  A S Bassett, E W C Chow, J Husted, K A Hodgkinson, E Oechslin, L Harris, C Silversides
• A new nonsense mutation of SMAD8 associated with pulmonary arterial hypertension

  (11 February, 2009)

  M Shintani, H Yagi, T Nakayama, T Saji, R Matsuoka