Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8 von Boycott, Kym M., Beaulieu, Chandree L., Kernohan, Kristin D., Gebril, Ola H., Mhanni, Aziz, Chudley, Albert E., Redl, David, Qin, Wen, Hampson, Sarah, Küry, Sébastien, Tetreault, Martine, Puffenberger, Erik G., Scott, James N., Bezieau, Stéphane, Reis, André, Uebe, Steffen, Schumacher, Johannes, Hegele, Robert A., McLeod, D. Ross, Gálvez-Peralta, Marina, Majewski, Jacek, Ramaekers, Vincent T., Nebert, Daniel W., Innes, A. Micheil, Parboosingh, Jillian S., Abou Jamra, Rami

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Public Sector Accounting Reform at Local Government Level in Indonesia von McLeod, Ross H., Harun, Harun

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Mutations in SRCAP, Encoding SNF2-Related CREBBP Activator Protein, Cause Floating-Harbor Syndrome von Hood, Rebecca L., Lines, Matthew A., Nikkel, Sarah M., Schwartzentruber, Jeremy, Beaulieu, Chandree, Nowaczyk, Małgorzata J.M., Allanson, Judith, Kim, Chong Ae, Wieczorek, Dagmar, Moilanen, Jukka S., Lacombe, Didier, Gillessen-Kaesbach, Gabriele, Whiteford, Margo L., Quaio, Caio Robledo D.C., Gomy, Israel, Bertola, Debora R., Albrecht, Beate, Platzer, Konrad, McGillivray, George, Zou, Ruobing, McLeod, D. Ross, Chudley, Albert E., Chodirker, Bernard N., Marcadier, Janet, Majewski, Jacek, Bulman, Dennis E., White, Susan M., Boycott, Kym M.

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TMEM237 Is Mutated in Individuals with a Joubert Syndrome Related Disorder and Expands the Role of the TMEM Family at the Ciliary Transition Zone von Huang, Lijia, Szymanska, Katarzyna, Jensen, Victor L., Janecke, Andreas R., Innes, A. Micheil, Davis, Erica E., Frosk, Patrick, Li, Chunmei, Willer, Jason R., Chodirker, Bernard N., Greenberg, Cheryl R., McLeod, D. Ross, Bernier, Francois P., Chudley, Albert E., Müller, Thomas, Shboul, Mohammad, Logan, Clare V., Loucks, Catrina M., Beaulieu, Chandree L., Bowie, Rachel V., Bell, Sandra M., Adkins, Jonathan, Zuniga, Freddi I., Ross, Kevin D., Wang, Jian, Ban, Matthew R., Becker, Christian, Nürnberg, Peter, Douglas, Stuart, Craft, Cheryl M., Akimenko, Marie-Andree, Hegele, Robert A., Ober, Carole, Utermann, Gerd, Bolz, Hanno J., Bulman, Dennis E., Katsanis, Nicholas, Blacque, Oliver E., Doherty, Dan, Parboosingh, Jillian S., Leroux, Michel R., Johnson, Colin A., Boycott, Kym M.

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An Evaluation of Some Key Economic Policies von McLeod, Ross H., Rosdaniah, Sitta

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Postoperative C‐reactive protein concentrations to predict infective complications following gastrectomy for cancer von Winsen, Marjolein, McSorley, Stephen T., McLeod, Ross, MacDonald, Andrew, Forshaw, Matthew J., Shaw, Martin, Puxty, Kathryn

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Unique pathways downstream of TLR-4 and TLR-7 activation: sex-dependent behavioural, cytokine, and metabolic consequences von Dunstan, Isobel K, McLeod, Ross, Radford-Smith, Daniel E, Xiong, Wenzheng, Pate, Trinity, Probert, Fay, Anthony, Daniel C

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High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome von Aretz, Stefan, Stienen, Dietlinde, Uhlhaas, Siegfried, Loff, Steffan, Back, Walter, Pagenstecher, Constanze, McLeod, D. Ross, Graham, Gail E., Mangold, Elisabeth, Santer, René, Propping, Peter, Friedl, Waltraut

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Civil society organisations' contribution to the anti-corruption movement in Indonesia von Setiyono, Budi, McLeod, Ross H.

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Survey of recent developments von McLeod, Ross H.

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Haploinsufficiency of HDAC4 Causes Brachydactyly Mental Retardation Syndrome, with Brachydactyly Type E, Developmental Delays, and Behavioral Problems von Williams, Stephen R., Aldred, Micheala A., Der Kaloustian, Vazken M., Halal, Fahed, Gowans, Gordon, McLeod, D. Ross, Zondag, Sara, Toriello, Helga V., Magenis, R. Ellen, Elsea, Sarah H.

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Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia von André, Jean-Luc, Lama, Giuliana, Joseph, Mark, Loirat, Chantal, Illies, Friederike, Bogdanovic, Radovan, Milford, David V, Saraiva, Jorge M, Stein, Anja, Takashima, Hiroshi, Tizard, Jane, Rosenbarker, Lisa, Cockfield, Sandra, Petty, Elizabeth M, John, Joy, Burguet, Antoine, Schmidt, Beate, Smith, Graham C, Lupski, James R, Weksberg, Rosanna, Cordeiro, Isabel, Yan, Jiong, Fründ, Stefan, Stankiewicz, Pawel, McLeod, D. Ross, Stockton, David W, Rodrigo, Francisco, Kaitila, Ilkka, Spranger, Jürgen, Thiele, Hannelore, Boerkoel, Cornelius F

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The struggle to regain effective government under democracy in Indonesia von Mcleod, Ross H.

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SURVEY OF RECENT DEVELOPMENTS von McLeod, Ross H.

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Generation and analysis of innovative genomically humanized knockin SOD1, TARDBP (TDP-43), and FUS mouse models von Devoy, Anny, Price, Georgia, De Giorgio, Francesca, Bunton-Stasyshyn, Rosie, Thompson, David, Gasco, Samanta, Allan, Alasdair, Codner, Gemma F., Nair, Remya R., Tibbit, Charlotte, McLeod, Ross, Ali, Zeinab, Noda, Judith, Marrero-Gagliardi, Alessandro, Brito-Armas, José M., Williams, Chloe, Öztürk, Muhammet M., Simon, Michelle, O'Neill, Edward, Bryce-Smith, Sam, Harrison, Jackie, Atkins, Gemma, Corrochano, Silvia, Stewart, Michelle, Gilthorpe, Jonathan D., Teboul, Lydia, Acevedo-Arozena, Abraham, Fisher, Elizabeth M.C., Cunningham, Thomas J.

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Exome Sequencing Identifies a Novel Variant in ACTC1 Associated With Familial Atrial Septal Defect von Greenway, Steven C., MD, McLeod, Ross, MD, Hume, Stacey, PhD, Roslin, Nicole M., MSc, Alvarez, Nanette, MD, Giuffre, Michael, MD, Zhan, Shing H., BSc, Shen, Yaoqing, PhD, Preuss, Christoph, PhD, Andelfinger, Gregor, MD, PhD, Jones, Steven J.M., PhD, Gerull, Brenda, MD

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In this issue: notes from the editor von McLeod, Ross H.

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Inadequate budgets and salaries as instruments for institutionalizing public sector corruption in Indonesia von McLeod, Ross H.

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In this issue: notes from the editor von McLeod, Ross H.

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Infantile Ictal Apneas in a Child With Williams-Beuren Syndrome von Myers, Kenneth A., MD, PhD, McLeod, D. Ross, MD, Bello-Espinosa, Luis, MD

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