Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia von Huang, Lijia, Chardon, Jodi Warman, Carter, Melissa T, Friend, Kathie L, Dudding, Tracy E, Schwartzentruber, Jeremy, Zou, Ruobing, Schofield, Peter W, Douglas, Stuart, Bulman, Dennis E, Boycott, Kym M

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Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia von Huang, Lijia, Warman-Chardon, Jodi, Carter, Melissa T, Friend, Kathie L, Dudding, Tracy E, Schwartzentruber, Jeremy, Zou, Ruobing, Schofield, Peter W, Douglas, Stuart, Bulman, Dennis E, Boycott, Kym M

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Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis von Buiting, Karin, Dittrich, Bärbel, Groß, Stephanie, Lich, Christina, Färber, Claudia, Buchholz, Tina, Smith, Ellie, Reis, André, Bürger, Joachim, Nöthen, Markus M., Barth-Witte, Ulli, Janssen, Bart, Abeliovich, Dvorah, Lerer, Israela, van den Ouweland, Ans M.W., Halley, Dicky J.J., Schrander-Stumpel, Connie, Smeets, Hubert, Meinecke, Peter, Malcolm, Sue, Gardner, Anne, Lalande, Marc, Nicholls, Robert D., Friend, Kathie, Schulze, Astrid, Matthijs, Gert, Kokkonen, Hannaleena, Hilbert, Pascale, Van Maldergem, Lionel, Glover, Guillermo, Carbonell, Pablo, Willems, Patrick, Gillessen-Kaesbach, Gabriele, Horsthemke, Bernhard

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