Genetic mutation in pontocerebellar hypoplasia

Supporting Information Additional Supporting Information may be found in the online version of this article. Fig. S1. Pedigree of the MSU pontocerebellar hypoplasias family 1 (PCHF1). The black symbols indicate children affected with PCH, the grey symbols indicate undiagnosed death in childhood of three paternal aunts who had history suggestive of profound developmental delays. Table S1. Genetic loci for pontocerebellar hypoplasias and single-nucleotide polymorphisms investigated Supporting information is available as part of the online article at http://www.blackwell-synergy.com Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.