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June 16, 2004BrainOpen Access

Homozygosity for CCTG mutation in myotonic dystrophy type 2

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Authors

BSBenedikt SchoserFriedrich Baur Stiftung

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Benedikt Schoser (2004) studied this question.

synapsesocial.com/papers/6a2158a9a2a97f3a085afa05https://doi.org/10.1093/brain/awh210
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular Dystrophy1992 · 1,472 citations
  2. 2Huntington disease expansion mutations in humans can occur before meiosis is completed2003 · 104 citations
  3. 3Proximal Myotonic Myopathy with MRI White Matter Abnormalities of the Brain1997 · 90 citations
  4. 4Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course2003 · 205 citations
  5. 5Muscle pathology in 57 patients with myotonic dystrophy type 22004 · 95 citations