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A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
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Haplotype study in Dutch SCA3 and SCA6 families: evidence for common founder mutations

Dineke S Verbeek1, Sytse J Piersma, Eric F A M Hennekam

  • 1Department of Medical Genetics, University Medical Center, Stratenum, Universiteitsweg 100, 3584 CG Utrecht, The Netherlands. D.S.Verbeek@med.uu.nl

European Journal of Human Genetics : EJHG
|March 18, 2004
PubMed

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